20682827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: non coding transcript exon variant
orthologous variants: 8337835-T-C

20682945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: non coding transcript exon variant
orthologous variants: 8337731-C-G

20683213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: non coding transcript exon variant
orthologous variants: 8337558-A-G

20683548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8337393-T-G

20684113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8336671-T-C

20684145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8336639-G-T

20684177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8336604-C-G

20684216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8336566-C-T

20684217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8336565-A-G

20684307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8336506-C-G

20684307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8336506-C-T

http://identifiers.org/hco/2/GRCh38#20684326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8336487-C-A

20684357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8336456-C-G

20684620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8336347-G-T

http://identifiers.org/hco/2/GRCh38#20684662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8336314-C-A

20684663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8336313-A-G

20684663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8336313-A-T

20684693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8336288-A-G

http://identifiers.org/hco/2/GRCh38#20684719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8336262-C-A

20684719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8336262-C-G

http://identifiers.org/hco/2/GRCh38#20684731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8336249-C-A

20684731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8336249-C-T

http://identifiers.org/hco/2/GRCh38#20684738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8336242-C-A

20684738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8336242-C-G

20684738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8336242-C-T

http://identifiers.org/hco/2/GRCh38#20684761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8336213-C-A

20684761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8336213-C-G

20684761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8336213-C-T

http://identifiers.org/hco/2/GRCh38#20684764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8336210-C-A

http://identifiers.org/hco/2/GRCh38#20684875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8336079-C-A

20684875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 8336079-C-T

20684887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8336022-G-A

http://identifiers.org/hco/2/GRCh38#20685042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8335769-C-A

20685068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8335743-A-G

20685091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8335720-G-C

20685091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8335720-G-T

20685092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8335719-G-A

20685092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8335719-G-T

20685191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8335660-G-A

20685191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8335660-G-T

http://identifiers.org/hco/2/GRCh38#20685231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8335621-A-C

20685234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8335618-T-A

20685234-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8335618-T-G

20685271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8335580-T-C

http://identifiers.org/hco/2/GRCh38#20685308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8335540-C-A

20685308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8335540-C-T

http://identifiers.org/hco/2/GRCh38#20685342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8335507-C-A

20685342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8335507-C-T

20685343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8335506-T-C

20685344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8335505-T-C

http://identifiers.org/hco/2/GRCh38#20685349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8335500-C-A

http://identifiers.org/hco/2/GRCh38#20685391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8335454-C-A

20685391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8335454-C-G

20685391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8335454-C-T

20685434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8335447-T-C

20685440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8335441-T-C

20685440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8335441-T-G

http://identifiers.org/hco/2/GRCh38#20685479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8335405-C-A

20685479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8335405-C-T

20685485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8335399-G-A

20685549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 8335320-A-G

20685576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8335294-T-G

http://identifiers.org/hco/2/GRCh38#20685612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8335259-A-C

20685681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8335185-G-T

http://identifiers.org/hco/2/GRCh38#20685763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8335072-C-A

20685763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8335072-C-T

20685789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8335050-T-C

20685789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8335050-T-G

20685811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8335028-A-G

20685848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8334989-T-C

20685953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8334892-T-C

http://identifiers.org/hco/2/GRCh38#20685964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8334881-A-C

20686368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8334522-G-A

20686368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8334522-G-T

20686896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8334098-G-T

http://identifiers.org/hco/2/GRCh38#20687009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8333983-A-C

http://identifiers.org/hco/2/GRCh38#20687052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/12/GRCm39#8333940-C-A

20687052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8333940-C-T

http://identifiers.org/hco/2/GRCh38#20687147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8333855-C-A

20687156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8333848-C-T

http://identifiers.org/hco/2/GRCh38#20687159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8333845-C-A

20687160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8333844-A-G

http://identifiers.org/hco/2/GRCh38#20687186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8333818-C-A

20687197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8333812-G-T

http://identifiers.org/hco/2/GRCh38#20687220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8333795-C-A

20687235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8333787-G-T

20687236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8333786-G-A

20687236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8333786-G-T

20687430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8333614-T-C

20687771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8333279-T-C

20687812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8333228-T-C

20694634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8332853-G-A

20694667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8332822-G-A

http://identifiers.org/hco/2/GRCh38#20694691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8332797-C-A

20694732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8332760-T-C

20694916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8332603-G-C

20694963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8332558-G-A

http://identifiers.org/hco/2/GRCh38#20695170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8332380-C-A

20695171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8332379-C-T

20695429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8332171-G-C

20695808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8332095-T-C

20695821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8332084-A-G

20695872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8332043-G-A

20695903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8332023-G-T

20695941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8331981-C-T

20696317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8331605-G-T

20696382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8331532-C-T

20696695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8331248-T-C

20697741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8330181-G-A

20697741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8330181-G-C

http://identifiers.org/hco/2/GRCh38#20697915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8330052-C-A

20698056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8329909-G-C

20698417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8329559-C-T

20698530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8329451-A-G

20698605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8329401-G-A

20699146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8328905-A-T

20699296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8328758-G-A

20699449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8328617-C-T

20699484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8328581-G-A

20699484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8328581-G-T

20699499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8328575-C-T

20699556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8328510-G-A

20699884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8328154-C-T

20700281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8327770-A-G

20700364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8327688-T-C

20701691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8325757-A-G

20701748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8325697-T-C

http://identifiers.org/hco/2/GRCh38#20701757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8325688-C-A

20701796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8325652-G-A

20701796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8325652-G-T

20701799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8325649-A-G

20701799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8325649-A-T

20725352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8324452-T-C

20725444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8324368-G-A

20725591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8324265-T-C

20725660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8324215-G-A

20725674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8324201-A-G

20725697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8324187-G-A

20725730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8324146-T-C

20726428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8323585-G-C

20726557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8323464-A-G

20726909-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8323105-A-T

20727064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8323043-T-C

20727236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8323013-A-T

20727256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8322993-T-G

20727359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8322898-C-T

20727982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8321877-G-T

http://identifiers.org/hco/2/GRCh38#20728239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8321621-C-A

http://identifiers.org/hco/2/GRCh38#20729185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8319781-C-A

20729393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8319590-C-T

20739554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8319271-C-T

http://identifiers.org/hco/2/GRCh38#20739581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8319241-C-A

20739729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8318826-T-C

20739819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8318730-T-C

20739826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8318723-A-T

20739899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8318664-A-G

20739991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8318576-A-G

20740351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8318222-C-T

20746473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8310264-G-T

20746790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8309928-T-C

20746790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8309928-T-G

http://identifiers.org/hco/2/GRCh38#20747205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8308975-C-A

20747282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8308901-T-C

20747429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8308766-G-T

20747474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8308731-A-G

20747536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8308684-G-A

20747804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8308107-A-G

20747844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8308069-T-C

20747959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8307952-A-G

20748540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8307528-G-A

20748640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8307441-T-C

20749181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8306392-T-G

20749325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8306257-T-C

20749398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8306190-T-C

20749587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8306043-T-C

20749607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8306025-G-A

20759505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8301987-T-C

20759517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8301975-A-G

http://identifiers.org/hco/2/GRCh38#20759635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8301871-C-A

20759635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8301871-C-T

20759697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8301819-T-C

20759979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8301550-G-A

20759979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8301550-G-T

20760079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8301456-T-C

20760180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8301382-A-G

20760229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8301336-G-A

20760495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8301093-A-T

http://identifiers.org/hco/2/GRCh38#20760647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8300945-C-A

20760973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8300675-A-G

20761218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8300464-T-C

20761286-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8300388-T-A

20764153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8297459-A-T

20764630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8296951-A-G

20764639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8296942-C-T

20768715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8295421-T-C

20768791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8295351-T-C

20768825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8295317-T-G

20768936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8295213-G-A

20769064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8295110-G-A

20769064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8295110-G-C

20769167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8295022-G-T

20769502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8294682-A-G

20769509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8294675-C-T

20769539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8294642-C-T

20769541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8294640-C-T

20769684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8294498-T-C

20769838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8294200-T-C

20770118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8293936-A-G

20770261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8293806-A-G

20770261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8293806-A-T

20770263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8293804-T-A

20770269-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8293798-T-A

20770269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8293798-T-C

http://identifiers.org/hco/2/GRCh38#20770283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8293785-A-C

20770310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8293757-A-G

20770374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8293713-T-C

20770455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8293641-T-C

20770730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8293187-C-T

20770861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8293079-C-T

20770988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8292989-T-C

20771269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8292534-G-A

20771269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8292534-G-C

20771545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8292260-G-A

20771545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8292260-G-C

20771643-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8292161-A-T

20772982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8291237-G-A

http://identifiers.org/hco/2/GRCh38#20773305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8290952-C-A

20773337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8290926-T-A

20773651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8290646-A-T

20773695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8290604-G-A

http://identifiers.org/hco/2/GRCh38#20773738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8290560-A-C

20774112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8290288-T-C

20774190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8290224-T-C

20774292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8290038-T-G

20774345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8289984-G-A

20774666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8288694-A-T

http://identifiers.org/hco/2/GRCh38#20774686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8288674-C-A

20774689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8288671-A-G

20775019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8288398-G-A

20775019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8288398-G-T

20775081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8288318-T-A

20775081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8288318-T-C

20775089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8288310-C-T

20775094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8288305-G-T

20775100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8288299-C-G

20775102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8288297-G-T

http://identifiers.org/hco/2/GRCh38#20775131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8288266-C-A

20775131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8288266-C-G

20775146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8288251-A-G

20775206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8288208-T-C

20775246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8288169-G-C

20775391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8288028-C-G

20775429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8287991-T-G

http://identifiers.org/hco/2/GRCh38#20775510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8287919-C-A

20775510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8287919-C-G

20775593-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8287849-T-G

20775636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8287812-A-G

20775714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8287743-G-A

20778790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8285514-C-T

20778855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8285468-T-C

http://identifiers.org/hco/2/GRCh38#20779542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8285069-C-A

http://identifiers.org/hco/2/GRCh38#20779863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8284804-A-C

http://identifiers.org/hco/2/GRCh38#20780091-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8284580-A-C

20780192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8284496-T-C

20780824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8283839-T-A

20781515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8283195-T-C

20781541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8283166-T-C

20781742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8282989-G-A

20787716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8278525-T-A

20787761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8278478-A-G

20787996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8278260-C-T

20788020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8278236-A-G

20788341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8277963-G-A

http://identifiers.org/hco/2/GRCh38#20788702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8277665-C-A

http://identifiers.org/hco/2/GRCh38#20788716-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8277651-A-C

20790379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 8277237-G-T

20790402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 8277214-A-G

20790435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8277185-T-C

20790456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8277164-C-T

http://identifiers.org/hco/2/GRCh38#20790553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8277049-C-A

http://identifiers.org/hco/2/GRCh38#20793025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8275599-A-C

http://identifiers.org/hco/2/GRCh38#20793199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8275424-A-C

20793199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8275424-A-T

20793656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8274971-T-C

20793669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8274958-A-G

20793911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8274732-A-G

http://identifiers.org/hco/2/GRCh38#20796654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#8273118-C-A

20796654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8273118-C-G

20796654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8273118-C-T

20796855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8272809-C-T

http://identifiers.org/hco/2/GRCh38#20796987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8272643-C-A

20796987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8272643-C-T

20796995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8272635-A-G

20797156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8272487-A-G

20801174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8270852-G-T

20801229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8270809-T-C

20801300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8270763-T-C

20801309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 8270754-C-T

20801427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8270636-C-G

20801458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 8270605-G-A

20801458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8270605-G-C

http://identifiers.org/hco/2/GRCh38#20801588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8270318-A-C

20801592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8270314-G-A

20801610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8270295-T-C

20802079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8269787-T-A

20802261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8269635-T-C

http://identifiers.org/hco/2/GRCh38#20802304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8269608-C-A

20802304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8269608-C-T

20802313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8269599-G-A

20802676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8269359-C-T

20802709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8269330-T-C

20802709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8269330-T-G

http://identifiers.org/hco/2/GRCh38#20802771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8269276-C-A

20802771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8269276-C-T

20802965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8269077-G-A

20803496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8268820-C-T

20803694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8268613-C-T

20803812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8268497-G-A

20803894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8268417-T-C

20804084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8268053-T-A

20804514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8267556-G-A

20804514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8267556-G-T

20804582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8267508-G-A

20805059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8267074-T-A

20805063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8267070-T-C

http://identifiers.org/hco/2/GRCh38#20805127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8266971-A-C

20805177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8266912-C-G

20805206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8266883-T-C

20805413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8266728-C-T

20805550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8266623-C-G

20805550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8266623-C-T

20805590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8266583-A-G

20805835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8266291-C-G

20805835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8266291-C-T

20806060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8266015-T-A

http://identifiers.org/hco/2/GRCh38#20806551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8265371-C-A

20806551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8265371-C-T

20807213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8262788-C-T

20807214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8262787-A-G

20807229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8262772-T-C

20807376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8262642-A-T

20807632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8262357-C-T

20807870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8262114-T-A

http://identifiers.org/hco/2/GRCh38#20807935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8262055-C-A

20807935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8262055-C-T

http://identifiers.org/hco/2/GRCh38#20808684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8261461-A-C

20808720-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8261421-T-A

20808778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8261356-A-G

20808876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8261247-C-T

20808891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8261232-T-C

http://identifiers.org/hco/2/GRCh38#20809037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8261028-C-A

20809037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8261028-C-T

20809631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8260547-T-C

20809734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8260429-C-T

http://identifiers.org/hco/2/GRCh38#20809772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8260392-A-C

20810105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8259529-G-C

20810315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8259321-A-G

20811358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26145
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8259148-G-T