http://identifiers.org/hco/2/GRCh38#28894694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#71923251-C-A

28894694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 71923251-C-G

28894694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 71923251-C-T

28894724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: missense_variant, undefined
orthologous variants: 71923281-G-A

28894748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: missense variant
orthologous variants: 71923305-T-C

28894902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: synonymous_variant, undefined
orthologous variants: 71923459-G-A

28894902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: synonymous_variant, undefined
orthologous variants: 71923459-G-T

28894944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, undefined
orthologous variants: 71923504-C-T

http://identifiers.org/hco/2/GRCh38#28894995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71923552-C-A

28894995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71923552-C-T

28895020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, undefined
orthologous variants: 71923583-T-A

28895020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, undefined
orthologous variants: 71923583-T-C

28895026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, undefined
orthologous variants: 71923589-G-A

28895026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, undefined
orthologous variants: 71923589-G-C

http://identifiers.org/hco/2/GRCh38#28895029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#71923592-C-A

28895029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, undefined
orthologous variants: 71923592-C-G

28895029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, undefined
orthologous variants: 71923592-C-T

http://identifiers.org/hco/2/GRCh38#28895033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#71923596-C-A

28895033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, undefined
orthologous variants: 71923596-C-T

http://identifiers.org/hco/2/GRCh38#28895049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71923614-C-A

28895049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71923614-C-T

http://identifiers.org/hco/2/GRCh38#28895075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#71923641-C-A

28895075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, undefined
orthologous variants: 71923641-C-G

28895075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, undefined
orthologous variants: 71923641-C-T

http://identifiers.org/hco/2/GRCh38#28895084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#71923650-C-A

28895084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, undefined
orthologous variants: 71923650-C-G

28895084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, undefined
orthologous variants: 71923650-C-T

28895100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 71923666-G-A

28895100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 71923666-G-T

28895171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 71923712-G-T

28895180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 71923721-G-A

28895180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 71923721-G-T

28895214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 71923756-T-G

28895288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 71923825-C-G

28895288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 71923825-C-T

http://identifiers.org/hco/2/GRCh38#28895306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#71923843-C-A

28895306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 71923843-C-G

28895306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 71923843-C-T

http://identifiers.org/hco/2/GRCh38#28895403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71923937-C-A

28895403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71923937-C-T

http://identifiers.org/hco/2/GRCh38#28895434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#71923968-C-A

28895434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, undefined
orthologous variants: 71923968-C-G

28895826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 71924229-A-G

28895853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 71924240-T-C

28895953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71924325-T-G

28895999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71924371-T-C

http://identifiers.org/hco/2/GRCh38#28896013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71924385-A-C

28896307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71924645-C-T

28896422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71924697-G-A

28896465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71924751-G-A

28897480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71926032-C-T

28897503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71926055-A-G

28897526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71926083-G-A

28897716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71926240-G-T

http://identifiers.org/hco/2/GRCh38#28897718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71926242-A-C

28899979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71929233-G-T

28900076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71929297-G-A

28901378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71931887-A-G

28901580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71932056-T-C

28901674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71932137-G-A

28901854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71932262-A-G

http://identifiers.org/hco/2/GRCh38#28901912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71932268-C-A

28901912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71932268-C-T

28901974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71932335-T-C

28902016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 71932377-A-G

28902064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: synonymous variant
orthologous variants: 71932425-A-G

http://identifiers.org/hco/2/GRCh38#28902169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71932527-C-A

28902169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71932527-C-T

28902216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71932568-G-A

28902216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71932568-G-T

28902223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71932575-G-A

28902223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71932575-G-C

28902223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71932575-G-T

28902390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71932712-A-G

28902416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71932737-A-G

28902498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71932802-G-A

28902747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71933026-A-G

28902946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71933202-A-G

http://identifiers.org/hco/2/GRCh38#28903019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71933274-C-A

28906643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71933947-G-A

28906643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71933947-G-T

http://identifiers.org/hco/2/GRCh38#28906694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71933998-C-A

28906694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71933998-C-G

28906717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71934021-A-T

28906947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71934228-G-C

28908511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71934599-C-T

28908533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71934614-A-G

28908579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71934643-T-C

28910361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71936467-G-A

28910361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71936467-G-C

28910364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71936470-G-A

28910611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71936688-A-G

28912119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71936803-G-T

28912309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71936948-T-G

28912327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71936966-A-G

28912342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71936981-T-C

28912342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71936981-T-G

28912551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71937118-T-C

28912748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71937315-A-G

28913516-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71938160-A-T

28913565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71938213-A-G

28913565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71938213-A-T

28913696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71938308-G-A

28913696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71938308-G-T

http://identifiers.org/hco/2/GRCh38#28913788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71938416-C-A

28913799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71938503-G-A

28913799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71938503-G-T

28913812-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71938516-A-T

28914031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71938963-T-C

28914182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: synonymous variant
orthologous variants: 71939110-A-G

28914188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: missense variant
orthologous variants: 71939116-T-A

http://identifiers.org/hco/2/GRCh38#28914249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71939181-A-C

http://identifiers.org/hco/2/GRCh38#28914331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71939259-C-A

28914350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71939277-T-G

http://identifiers.org/hco/2/GRCh38#28917876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71940602-C-A

28917876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71940602-C-G

28917876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71940602-C-T

28917878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71940604-G-C

28917878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71940604-G-T

http://identifiers.org/hco/2/GRCh38#28917899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71940625-C-A

28917899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: synonymous variant
orthologous variants: 71940625-C-G

28917899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: synonymous variant
orthologous variants: 71940625-C-T

28917974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: synonymous variant
orthologous variants: 71940700-T-A

28917974-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: synonymous variant
orthologous variants: 71940700-T-G

http://identifiers.org/hco/2/GRCh38#28918034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71940758-C-A

28918082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71941685-G-A

28918082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71941685-G-C

28918089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71941692-A-G

http://identifiers.org/hco/2/GRCh38#28922837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71943471-A-C

28922837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71943471-A-G

28922837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71943471-A-T

28922848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71943482-G-A

28922848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71943482-G-T

28923000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71943633-C-T

28923017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71943656-T-C

28923190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71943834-A-G

28923210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71943856-G-A

28923266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71943889-C-T

28923301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71943900-G-A

28923333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71943926-T-G

http://identifiers.org/hco/2/GRCh38#28923897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71944459-A-C

28923901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71944463-G-A

28923957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71944521-G-A

28923957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71944521-G-T

28924262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71944758-G-A

http://identifiers.org/hco/2/GRCh38#28924389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71944824-C-A

28924389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71944824-C-T

28924644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71945041-G-A

http://identifiers.org/hco/2/GRCh38#28924839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71945212-C-A

28924839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71945212-C-T

28924875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron variant
orthologous variants: 71945237-A-G

28925306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71945611-G-T

28925518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71945774-T-C

28926265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71947094-C-G

28926268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71947097-T-A

28926302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71947128-G-A

28926406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71947180-G-T

28926418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71947192-T-C

28926446-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71947209-T-A

28926446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71947209-T-C

28926446-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71947209-T-G

28926571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71947332-T-A

28926571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71947332-T-C

28926615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71947371-T-C

28926642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71947410-G-A

28926642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71947410-G-T

28926922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71947741-A-G

28926929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71947744-A-G

28926950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71947767-G-T

28927020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71947830-T-C

28927176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71947980-G-T

28927183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71947987-G-A

http://identifiers.org/hco/2/GRCh38#28927187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71947991-A-C

http://identifiers.org/hco/2/GRCh38#28927419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71948119-C-A

28927453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71948165-A-T

28927462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71948174-G-C

28927462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71948174-G-T

28927509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71948224-G-T

28927537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71948252-T-C

28927539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71948254-T-C

28927551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71948266-G-A

28927551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71948266-G-T

28927552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71948267-C-T

28927554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71948269-A-G

28927618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71948331-T-G

28927696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71948409-A-T

28927748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71948441-A-G

http://identifiers.org/hco/2/GRCh38#28927755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71948448-A-C

28927802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71948481-T-G

http://identifiers.org/hco/2/GRCh38#28927817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71948496-C-A

28927817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71948496-C-T

http://identifiers.org/hco/2/GRCh38#28927866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71948525-A-C

28927866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71948525-A-G

28929343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71949514-A-G

http://identifiers.org/hco/2/GRCh38#28929377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71949546-A-C

28929398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71949561-A-G

28929414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71949577-T-C

28929543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71949667-T-A

28929543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71949667-T-C

28929851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71949957-T-A

28930007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71950092-T-C

28930010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71950095-A-G

28930010-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71950095-A-T

28930101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71950186-T-C

28930174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71950255-A-G

28930344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71950392-G-A

28930434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71950474-T-C

28930591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71950668-A-G

28930768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71950818-G-A

28930790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71950832-C-T

http://identifiers.org/hco/2/GRCh38#28930822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71950864-C-A

28930822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71950864-C-T

28930850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71950895-T-A

28930850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71950895-T-G

28933965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71952510-G-A

28934004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71952545-C-T

28934118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71952613-A-G

28934145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71952640-T-C

28934265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71952751-G-A

28934265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71952751-G-C

28934589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71953049-C-T

28935343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71955617-C-T

28935349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71955623-A-G

http://identifiers.org/hco/2/GRCh38#28935373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71955637-C-A

28935373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71955637-C-T

http://identifiers.org/hco/2/GRCh38#28935395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71955662-C-A

28935395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71955662-C-T

28935398-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71955665-T-G

28935406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71955673-T-C

28935406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71955673-T-G

28935408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71955675-A-T

28935409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71955676-T-A

28935409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71955676-T-C

28935411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71955678-G-A

28935411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71955678-G-T

http://identifiers.org/hco/2/GRCh38#28935412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71955679-C-A

28935416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71955683-G-T

28935433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71955694-A-G

28935433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71955694-A-T

28935460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71955710-T-A

28935460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71955710-T-C

28935490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71955738-T-C

28936154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71956303-A-G

http://identifiers.org/hco/2/GRCh38#28936525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71956615-C-A

28936577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71956666-T-C

28936630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71956728-T-G

28936657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71956751-T-C

28936844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71956933-T-C

http://identifiers.org/hco/2/GRCh38#28936849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71956938-A-C

28936849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71956938-A-G

28936879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71956970-G-A

28936879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71956970-G-T

28936948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71957038-T-A

28936948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71957038-T-C

28936969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71957059-T-A

28936969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71957059-T-C

28937894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71957521-T-G

28940997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71959375-A-G

28940997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71959375-A-T

28941054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71959426-G-A

28941065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71959437-T-G

28941437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71959742-C-G

28941589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71959904-T-C

28941598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71959913-G-A

28941598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71959913-G-C

28941598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71959913-G-T

28941614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71959927-A-G

28941617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71959930-G-A

28941654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71959967-A-G

28942118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71960278-T-C

28942135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71960296-A-G

28942162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71960321-T-C

28942227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71960370-G-T

28946062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71963980-G-A

28946062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71963980-G-T

28946206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71964146-G-T

28946264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71964208-T-G

28946472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71964358-T-A

28946472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71964358-T-C

28946493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71964379-T-G

http://identifiers.org/hco/2/GRCh38#28946526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71964407-A-C

28946526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71964407-A-G

28946569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71964442-T-C

28946650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71964518-C-T

28946767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: synonymous variant
orthologous variants: 71964644-T-C

http://identifiers.org/hco/2/GRCh38#28946804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71964682-C-A

28947121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: 3 prime UTR variant
orthologous variants: 71965011-C-T

28947130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: 3 prime UTR variant
orthologous variants: 71965020-G-A

28947130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: 3 prime UTR variant
orthologous variants: 71965020-G-T

http://identifiers.org/hco/2/GRCh38#28947240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71965128-A-C

28947749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28945
most severe consequence: 3 prime UTR variant
orthologous variants: 71965604-T-G