44682201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69716757-G-T

44682244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69716800-G-T

44682273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69716828-A-G

44682310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69716869-T-A

44682310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69716869-T-C

44682348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 69716907-A-G

44682354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 69716913-A-G

44682363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 69716922-C-T

44682425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69716983-G-A

44682425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69716983-G-C

44682425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69716983-G-T

44682435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69716993-T-A

44682435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69716993-T-C

44682483-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69717045-T-A

44682483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69717045-T-C

44682500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69717085-G-C

44682500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69717085-G-T

http://identifiers.org/hco/4/GRCh38#44682541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#69717127-C-A

44682541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69717127-C-G

44682541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69717127-C-T

44682646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 69717227-T-C

44682653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69717234-G-C

44682653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69717234-G-T

44682674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69717256-A-G

44682684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69717266-G-C

44682684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69717266-G-T

44682706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69717278-G-A

44682706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69717278-G-T

44683288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 69717828-G-A

44683366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69718272-A-G

44683372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69718278-G-A

44683372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69718278-G-T

44683426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69718329-A-G

44686138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69718673-G-T

44686258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69718783-C-T

44686387-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69718900-A-T

44686388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69718901-T-A

44686388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69718901-T-C

44686393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69718906-G-A

44686393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69718906-G-T

http://identifiers.org/hco/4/GRCh38#44686697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#69719184-C-A

44686697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 69719184-C-T

44686794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69719259-G-A

44686794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69719259-G-T

http://identifiers.org/hco/4/GRCh38#44686835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#69719292-C-A

44686835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69719292-C-T

44686847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69719305-A-G

44687022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69719485-G-T

44687143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69719617-A-G

44687576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69720096-G-A

44687908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69720334-G-A

44687908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69720334-G-C

44687908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69720334-G-T

44687935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69720358-G-T

44688103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 69720522-G-A

44688181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69720599-T-C

44688210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69720627-G-C

44688518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69720947-G-C

44688640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69721078-C-T

44688645-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69721083-G-C

44688774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69721210-G-A

44688845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69721474-A-G

http://identifiers.org/hco/4/GRCh38#44689179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#69721804-A-C

44689206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69721831-A-G

44689214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69721839-G-A

44689214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69721839-G-C

44689214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69721839-G-T

44689248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69721844-G-A

44689365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 69721946-G-T

http://identifiers.org/hco/4/GRCh38#44689424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69722005-C-A

44689424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69722005-C-T

44689458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69722060-G-A

44689458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69722060-G-T

44689486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69722114-G-A

44689488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69722116-A-G

44689490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69722118-G-A

44689490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69722118-G-T

44689667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69722589-C-G

http://identifiers.org/hco/4/GRCh38#44689924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69722854-A-C

http://identifiers.org/hco/4/GRCh38#44689966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69722896-A-C

44690015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69722932-A-G

44690025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69722942-T-C

44690025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69722942-T-G

44690054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69722984-G-A

44690054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69722984-G-T

http://identifiers.org/hco/4/GRCh38#44690071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69723000-C-A

44690243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69723145-A-G

44690693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69723680-A-G

http://identifiers.org/hco/4/GRCh38#44690697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69723684-C-A

44690697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69723684-C-G

44690697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69723684-C-T

44690734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 69723721-A-G

44690743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 69723730-T-C

44690743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 69723730-T-G

44690824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 69723811-A-G

44690824-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 69723811-A-T

44690897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69723867-T-C

44690897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69723867-T-G

44690898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69723868-T-C

44690910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69723880-A-G

44691015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69723988-G-A

44691625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69724440-G-A

44691688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 69724493-A-G

44691688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 69724493-A-T

44691886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69724684-G-T

44692004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69724789-T-G

http://identifiers.org/hco/4/GRCh38#44692123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69724874-C-A

44692156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69724908-G-A

44693797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69725203-G-T

44693830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69725235-G-A

44693846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69725252-T-C

http://identifiers.org/hco/4/GRCh38#44693847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69725253-A-C

http://identifiers.org/hco/4/GRCh38#44694070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69725415-C-A

44694086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69725431-T-C

http://identifiers.org/hco/4/GRCh38#44694098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69725435-C-A

44694098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69725435-C-T

44694111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69725448-G-T

http://identifiers.org/hco/4/GRCh38#44694116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69725453-C-A

44694172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69725514-A-G

44694451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 69725778-T-G

http://identifiers.org/hco/4/GRCh38#44694521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69725848-C-A

44694521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 69725848-C-G

44694521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 69725848-C-T

44694579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69725914-G-T

44696205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69727056-A-G

http://identifiers.org/hco/4/GRCh38#44696271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69727122-C-A

44696271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69727122-C-T

44696850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69727579-A-G

44696888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69727623-C-G

44696920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69727653-C-T

44697089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69727829-A-G

44697198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69727935-T-C

44697496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69728182-T-C

44697557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69728233-G-A

44697557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69728233-G-T

http://identifiers.org/hco/4/GRCh38#44698434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69728833-A-C

44698434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69728833-A-T

44698642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 69729025-T-C

44698733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69729114-G-C

44698742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69729123-T-C

44702222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69732419-C-T

http://identifiers.org/hco/4/GRCh38#44702348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69732530-C-A

44702697-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69732866-T-A

44702697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69732866-T-C

http://identifiers.org/hco/4/GRCh38#44702759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69732922-C-A

44702864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69733003-T-C

44702879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69733014-T-A

44702879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69733014-T-C

44703054-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69733214-T-A

http://identifiers.org/hco/4/GRCh38#44703193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69733347-C-A

44703193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69733347-C-G

http://identifiers.org/hco/4/GRCh38#44703196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69733350-A-C

44703196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69733350-A-G

http://identifiers.org/hco/4/GRCh38#44703240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69733380-C-A

44703362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69733451-T-G

44703368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69733457-A-G

http://identifiers.org/hco/4/GRCh38#44703375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69733462-C-A

44703375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69733462-C-G

44703379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69733466-T-A

44703379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69733466-T-C

http://identifiers.org/hco/4/GRCh38#44703402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69733491-C-A

44703402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69733491-C-T

44703426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69733522-A-G

44703454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69733548-A-G

44703545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69733624-T-C

44703546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69733625-G-A

44703546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69733625-G-C

44703546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69733625-G-T

http://identifiers.org/hco/4/GRCh38#44703597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69733945-A-C

44703597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69733945-A-G

44703597-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69733945-A-T

44703611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69733984-T-A

44703625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69733998-A-G

http://identifiers.org/hco/4/GRCh38#44703671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69734042-C-A

44703671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69734042-C-G

44703794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69734164-C-T

44703849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69734216-T-C

44703859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69734232-G-T

44703945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69734331-C-T

44703972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69734361-G-T

44704046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69734424-A-G

44704119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69734491-A-G

44704185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69734545-A-G

44707268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69734917-G-T

44707288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69734941-T-C

44707393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69735045-G-A

44707393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69735045-G-T

44707503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69735132-T-C

44707555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69735152-T-C

44707604-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69735183-T-G

44707627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69735202-G-T

44707643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69735219-G-A

44707643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69735219-G-C

44707643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69735219-G-T

44707747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 69735316-C-T

44707756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 69735325-A-G

44707846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 69735415-A-G

http://identifiers.org/hco/4/GRCh38#44710676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69736608-A-C

44710806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69736735-G-A

44710824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69736753-A-G

http://identifiers.org/hco/4/GRCh38#44710836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69736761-C-A

44710836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69736761-C-T

44710843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69736768-T-C

44710931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69736832-G-A

44710931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69736832-G-T

44710938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69736839-A-G

44711180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69737082-G-A

44711180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69737082-G-C

44711180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69737082-G-T

http://identifiers.org/hco/4/GRCh38#44711218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69737141-A-C

44711218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69737141-A-G

44711218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69737141-A-T

44711270-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69737200-T-A

44711270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69737200-T-C

44711541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69737396-G-A

44711541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69737396-G-C

44711571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69737439-C-G

44711571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69737439-C-T

http://identifiers.org/hco/4/GRCh38#44711806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69737625-C-A

44711806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69737625-C-T

44711898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69737715-C-G

44711898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69737715-C-T

http://identifiers.org/hco/4/GRCh38#44711905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69737722-C-A

44711905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69737722-C-G

44711972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69737794-A-G

44712061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69737860-T-C

44712314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69738082-G-A

44712797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69738533-G-A

44712801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69738537-T-C

44712955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69738678-T-C

44713202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69738919-A-G

44713447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69739144-T-C

44714308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69739307-T-C

44714540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69739517-G-A

44714540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69739517-G-C

44714557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69739534-G-A

44714584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69739561-T-C

http://identifiers.org/hco/4/GRCh38#44714772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69739767-A-C

44715058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69740408-G-A

44715607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69740921-G-C

44716340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69741601-A-G

44716389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69741648-A-G

44716400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69741659-G-A

http://identifiers.org/hco/4/GRCh38#44716587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69741812-C-A

44716587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69741812-C-T

44716821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69742028-T-G

44716865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69742063-C-T

44716870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69742068-A-G

44716985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69742199-A-G

44717024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69742231-A-T

44717056-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69742257-T-A

44717056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69742257-T-C

44717057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69742258-A-G

44717057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69742258-A-T

44717335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69742539-T-C

44717335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69742539-T-G

44717337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69742541-A-G

44717593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69742745-A-G

44717623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69742773-T-C

44717778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69743312-C-T

44717890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69743425-A-T

44718117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69743710-C-G

http://identifiers.org/hco/4/GRCh38#44718172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69743735-C-A

44718172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69743735-C-T

44718291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69743790-T-A

44718295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69743794-T-C

44718303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69743802-G-T

44718381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 69743880-G-A

44718381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69743880-G-T

44718382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 69743881-T-C

44718447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69743946-T-C

44718453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69743952-T-C

http://identifiers.org/hco/4/GRCh38#44718466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69743966-C-A

44718468-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69743968-T-G

44718473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69743973-T-A

44718473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69743973-T-C

44718550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69744040-T-A

44718741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69744217-A-G

44718939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69744302-A-T

44719080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69744464-A-T

http://identifiers.org/hco/4/GRCh38#44719086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69744470-C-A

44719086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69744470-C-T

44719260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69744642-G-A

44719434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69744823-G-A

44719434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69744823-G-C

44719615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69744953-T-C

44719615-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69744953-T-G

44719948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69745051-A-G

http://identifiers.org/hco/4/GRCh38#44720024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69745110-C-A

44720024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69745110-C-G

44720256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69745339-T-C

44720314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69745398-G-A

44720334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69745418-C-T

44720407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69745485-C-G

http://identifiers.org/hco/4/GRCh38#44720630-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69745650-A-C

44720909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69745873-A-G

44720926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69745890-G-A

44721001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69745959-A-G

44721001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69745959-A-T

44721041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69745995-A-G

44721041-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69745995-A-T

44721048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69746002-T-A

44721207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69746167-C-G

44721215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69746175-G-A

http://identifiers.org/hco/4/GRCh38#44721237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69746197-A-C

44721286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69746249-A-G

44721312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69746290-C-T

44721387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69746376-G-A

44721476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69746456-A-G

44721506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69746476-T-C

44721517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69746488-G-A

44721686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69746641-G-A

44722032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69746956-G-T

44722121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 69747041-A-G

44722127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 69747047-G-A

44722479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69747387-T-C

44724608-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69748014-T-A

44724876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69748280-G-A

http://identifiers.org/hco/4/GRCh38#44724895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#69748299-A-C

44725050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69748449-G-A

44725056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69748455-C-T

44725461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69748822-G-A

44725461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69748822-G-C

http://identifiers.org/hco/4/GRCh38#44725957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#69749257-C-A

http://identifiers.org/hco/4/GRCh38#44726033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#69749333-C-A

http://identifiers.org/hco/4/GRCh38#44726420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#69749523-C-A

44726492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 69749570-T-C

44726501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 69749579-G-A

44726501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 69749579-G-T

44726534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 69749611-G-A

44726550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 69749627-G-A

44726550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21526
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 69749627-G-T