45454625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116386458-C-T

45454861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116386226-G-A

http://identifiers.org/hco/10/GRCh38#45454882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116386205-C-A

http://identifiers.org/hco/10/GRCh38#45455098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116386042-C-A

45455098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116386042-C-T

http://identifiers.org/hco/10/GRCh38#45455109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116386031-C-A

http://identifiers.org/hco/10/GRCh38#45455152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116385983-C-A

45455152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116385983-C-T

45455339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116385794-T-C

45455354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116385779-G-A

45455354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116385779-G-C

45455372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116385761-T-C

45455373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116385760-A-G

45455399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116385738-G-A

45455399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116385738-G-T

45455463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116385679-C-T

45455493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116385648-C-T

45455501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116385640-G-A

45455501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116385640-G-T

http://identifiers.org/hco/10/GRCh38#45455607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116385542-C-A

45455624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116385525-T-C

http://identifiers.org/hco/10/GRCh38#45455780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116385415-C-A

45455780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116385415-C-T

45455784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116385411-G-A

http://identifiers.org/hco/10/GRCh38#45455798-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116385397-A-C

45455894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116385341-G-A

http://identifiers.org/hco/10/GRCh38#45455988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116385246-C-A

45455995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116385239-T-A

45456167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116385134-G-A

45456241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116385083-G-T

45456394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116384960-C-T

45456409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116384946-A-G

45456576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116384803-T-C

http://identifiers.org/hco/10/GRCh38#45456655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116384730-C-A

45456655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116384730-C-G

45456655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116384730-C-T

45456809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116384581-G-T

45456854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116384532-A-G

45456883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116384503-G-C

45456921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116384467-C-T

45456986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116384412-G-A

45456986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116384412-G-T

http://identifiers.org/hco/10/GRCh38#45457035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116384359-C-A

45457149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116384305-G-A

45457149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116384305-G-C

45457149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116384305-G-T

45457218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116384236-G-C

45457220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116384234-A-G

45457249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3 prime UTR variant
orthologous variants: 116384205-A-G

45457539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116383970-A-G

45457559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116383951-G-C

45457626-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116383882-A-T

http://identifiers.org/hco/10/GRCh38#45457726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116383784-A-C

45457841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116383668-C-T

http://identifiers.org/hco/10/GRCh38#45457842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116383667-C-A

45457842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116383667-C-T

45457860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116383647-G-A

45457860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116383647-G-T

http://identifiers.org/hco/10/GRCh38#45457901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116383630-C-A

45457901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116383630-C-G

45457901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116383630-C-T

http://identifiers.org/hco/10/GRCh38#45457956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116383572-C-A

45457956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116383572-C-T

http://identifiers.org/hco/10/GRCh38#45458060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116383464-C-A

45458060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116383464-C-T

http://identifiers.org/hco/10/GRCh38#45458459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116383068-C-A

45459104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116382757-C-G

45459110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116382751-G-A

http://identifiers.org/hco/10/GRCh38#45459283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116382579-A-C

45459283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116382579-A-G

45459286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116382575-G-A

45459299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116382563-G-C

45459339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116382519-G-A

45459339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116382519-G-T

http://identifiers.org/hco/10/GRCh38#45459395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116382467-C-A

45459395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116382467-C-T

45459431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116382428-C-T

45459590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116382305-T-A

45459590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116382305-T-G

45459811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116381728-T-C

45459816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116381723-G-C

45459819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116381720-C-G

45459854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116381691-T-C

45459863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116381682-T-G

45459941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116381613-G-A

45459941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116381613-G-T

45459986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116381578-G-T

45460086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116381473-A-T

45460088-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116381471-A-T

45460244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116381323-T-C

45460486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116381098-T-C

45460947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116380780-C-T

45460974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116380752-G-T

45461069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116380684-A-G

45461118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116380643-C-T

45461172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116380595-C-T

http://identifiers.org/hco/10/GRCh38#45461220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#116380570-C-A

45461220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116380570-C-T

45461349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 116380441-C-T

http://identifiers.org/hco/10/GRCh38#45461430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116380361-C-A

45461430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116380361-C-G

http://identifiers.org/hco/10/GRCh38#45461523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116380266-A-C

45461523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116380266-A-G

http://identifiers.org/hco/10/GRCh38#45461580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116380209-A-C

http://identifiers.org/hco/10/GRCh38#45461714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116380086-A-C

45461841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116379969-G-T

http://identifiers.org/hco/10/GRCh38#45461878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116379933-A-C

45461894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116379917-T-C

http://identifiers.org/hco/10/GRCh38#45462165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116379672-C-A

45462206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116379614-A-G

http://identifiers.org/hco/10/GRCh38#45462297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116379552-C-A

45462297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116379552-C-T

45462309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116379541-G-A

45462309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116379541-G-T

45462332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116379522-G-A

45462332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116379522-G-T

45462393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116379449-G-C

http://identifiers.org/hco/10/GRCh38#45462534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116379392-C-A

45463339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116378953-C-T

45463473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116378819-G-A

45463523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116378769-G-C

45463644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116378648-G-T

45463826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116378466-T-C

45463826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116378466-T-G

45464086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116378209-G-A

45464086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116378209-G-C

45464086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116378209-G-T

45464113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116378183-A-G

45464318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116378005-G-A

45464318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116378005-G-T

45464332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116377991-A-T

45464338-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116377985-A-T

45464342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116377981-C-T

45464381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116377942-G-A

45464381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116377942-G-T

http://identifiers.org/hco/10/GRCh38#45464394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116377926-A-C

45464421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116377898-T-A

45464421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116377898-T-C

http://identifiers.org/hco/10/GRCh38#45464442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116377877-C-A

45464554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116377586-C-T

45464821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116377351-T-C

45465048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116377174-T-C

45465262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116376413-A-G

http://identifiers.org/hco/10/GRCh38#45465544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116376176-A-C

45470422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116375412-T-C

45470422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116375412-T-G

45470510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116375332-C-T

45470590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116375276-T-C

45470753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116375118-C-T

45470877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116375000-C-G

45471525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116374398-C-G

45471635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116374297-A-G

45471683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116374253-C-T

45471984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116373732-T-C

45473272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116372826-A-T

45473691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116372381-G-T

45473873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116372217-T-C

45473964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116372053-C-T

45474198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116371842-G-T

45484203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116371531-C-T

45484341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116371406-T-G

45484386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116371364-G-A

45489171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116369918-C-T

http://identifiers.org/hco/10/GRCh38#45489312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116369588-C-A

45489312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116369588-C-T

45489317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116369583-G-A

45489317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116369583-G-T

http://identifiers.org/hco/10/GRCh38#45489442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116369458-A-C

45489450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116369453-A-G

45489461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116369441-A-G

http://identifiers.org/hco/10/GRCh38#45489507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116369401-A-C

45489507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116369401-A-G

45489603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116369315-C-T

45511321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116364286-A-G

45513646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116363898-A-G

45514106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116363465-T-C

45514203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116363376-T-C

45514287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116363311-T-C

45514370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116363226-C-T

45514535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116363036-G-A

45514650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116362917-T-C

45514964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116362644-C-T

http://identifiers.org/hco/10/GRCh38#45515009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116362624-C-A

45515009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116362624-C-G

45515009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116362624-C-T

45524625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116357791-C-G

45524625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116357791-C-T

45524704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116357718-T-C

45524747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116357676-G-T

45524935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116357277-G-A

45525068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116357182-G-A

45525399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116356797-T-C

http://identifiers.org/hco/10/GRCh38#45525449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116356770-A-C

45531843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116354878-T-C

45532902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116354553-T-G

45532978-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116354478-T-A

45532978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116354478-T-C

45533020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116354438-C-T

45533030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116354429-G-C

http://identifiers.org/hco/10/GRCh38#45533323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116353624-C-A

45533402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116353564-G-A

45533402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116353564-G-T

45533674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116352943-T-C

45534583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116352073-A-G

45534741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116351948-C-T

45534776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116351913-C-G

45534776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116351913-C-T

45535081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116351632-T-C

45535233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116351487-T-C

http://identifiers.org/hco/10/GRCh38#45535311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116351423-C-A

45535348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116351386-T-C

45535360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116351374-T-C

45535430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116351303-G-A

45535549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116351190-A-G

45535777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116351016-A-G

45535927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116350878-T-C

45535990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116350715-G-A

45536263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116350452-C-T

http://identifiers.org/hco/10/GRCh38#45536272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116350443-A-C

45536289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116350425-C-G

45536592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116350074-A-G

45536592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116350074-A-T

45536950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116349888-C-T

45536954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116349885-T-G

45537345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116349526-G-A

http://identifiers.org/hco/10/GRCh38#45558138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116336709-A-C

45558274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116336606-G-T

45558352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116336534-T-C

45558811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116336190-T-C

45578476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116329975-G-A

45578641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116329845-G-A

45578862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116329643-G-A

45578862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116329643-G-T

45578973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116329538-T-C

45579455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116329084-T-G

45580232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116328438-T-C

45580686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116328000-A-G

http://identifiers.org/hco/10/GRCh38#45581046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116327703-A-C

45581058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116327691-G-A

http://identifiers.org/hco/10/GRCh38#45581391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116327433-C-A

45581391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116327433-C-G

45581853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116327007-C-T

45581883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116326979-C-T

45581918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116326944-G-A

45581918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116326944-G-C

http://identifiers.org/hco/10/GRCh38#45581940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116326917-C-A

45581940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116326917-C-G

45582906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116324476-A-G

45592963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116316621-T-C

45593020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116316574-C-T

45593025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116316569-T-G

45593435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116316173-A-G

45593463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116316139-T-C

45593514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116316100-C-T

45593638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116316018-G-A

45593666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116315992-T-C

45593957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116315736-G-T

45594228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116315457-T-C

http://identifiers.org/hco/10/GRCh38#45594320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116315374-C-A

45594320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116315374-C-T

45594365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116315321-G-A

45594365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116315321-G-T

45594370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116315316-A-G

45594394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116315291-C-T

45594434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116315261-A-T

45594719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116315128-C-G

45594719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116315128-C-T

45594810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 116315063-G-A

45594810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 116315063-G-T

http://identifiers.org/hco/10/GRCh38#45594812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#116315061-C-A

45594901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23356
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 116314987-A-G