36826920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 111224750-A-G

36827067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 111224617-A-T

http://identifiers.org/hco/3/GRCh38#36827079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111224606-C-A

36827079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 111224606-C-G

36827203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 111224506-G-T

36827205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 111224503-G-T

http://identifiers.org/hco/3/GRCh38#36827346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111224401-C-A

36827346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 111224401-C-T

36827360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 111224393-G-T

http://identifiers.org/hco/3/GRCh38#36827413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111224343-C-A

http://identifiers.org/hco/3/GRCh38#36827428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111224328-C-A

36827442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 111224314-G-A

36827442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 111224314-G-T

36827475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 111224282-G-A

36827497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 111224260-A-G

http://identifiers.org/hco/3/GRCh38#36827669-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111223999-A-C

36827669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 111223999-A-G

http://identifiers.org/hco/3/GRCh38#36827796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111223891-C-A

36827796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 111223891-C-T

36827875-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 111223814-T-A

36827875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 111223814-T-G

36828072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 111223632-T-C

36828087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 111223620-A-T

36828124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 111223573-G-T

36828234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 111223469-G-A

36828234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 111223469-G-C

36828234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 111223469-G-T

36828256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 111223447-G-C

36828256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 111223447-G-T

36828414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111223306-A-G

36828566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111223229-T-C

http://identifiers.org/hco/3/GRCh38#36829490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111222993-C-A

36829490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111222993-C-G

36829490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111222993-C-T

http://identifiers.org/hco/3/GRCh38#36829530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111222954-A-C

http://identifiers.org/hco/3/GRCh38#36829542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111222942-C-A

36829723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111222762-A-G

36830813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111222116-G-T

36830861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111222074-G-A

36831259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 111221673-T-G

36831404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 111221537-A-G

36831523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 111221409-C-T

36831661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 111221271-T-C

36831767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 111221165-G-C

36831767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 111221165-G-T

36831913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 111221019-C-T

36831955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 111220977-A-G

36832066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 111220866-A-G

36832219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 111220713-A-T

http://identifiers.org/hco/3/GRCh38#36832667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111220265-C-A

36832848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 111220084-G-A

36832848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 111220084-G-T

36833124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 111219808-T-C

http://identifiers.org/hco/3/GRCh38#36833418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111219514-C-A

36833418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 111219514-C-T

36833860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 111219072-C-T

36834053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111218887-A-T

36834295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111218805-G-A

36834295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111218805-G-T

36834301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111218799-C-G

36834301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111218799-C-T

36834438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 111218677-G-T

http://identifiers.org/hco/3/GRCh38#36834473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111218637-C-A

36834489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111218621-G-T

http://identifiers.org/hco/3/GRCh38#36834537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111218577-C-A

36834537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111218577-C-G

36834537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111218577-C-T

36834550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111218568-T-A

36834550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111218568-T-C

http://identifiers.org/hco/3/GRCh38#36834553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111218565-C-A

36834618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111218507-G-T

http://identifiers.org/hco/3/GRCh38#36834621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111218504-C-A

36834621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111218504-C-T

36834635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111218491-T-G

36834915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 111218216-G-A

36834949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111218184-A-T

36834964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111218172-T-C

36834964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111218172-T-G

http://identifiers.org/hco/3/GRCh38#36834980-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111218153-A-C

36835016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111218123-T-G

36836135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111217052-G-A

36837713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111216583-G-A

36838243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111215874-C-T

36838290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111215849-T-C

36838333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111215807-C-T

36838418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 111215724-G-A

36838505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, splice_acceptor_variant
orthologous variants: 111215637-C-T

36838751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111215402-T-G

http://identifiers.org/hco/3/GRCh38#36838827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111215333-C-A

36838827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111215333-C-T

36838877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111215284-G-A

36839309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111214842-G-A

36839795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111214374-T-G

36840192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111214036-T-C

36840522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111213772-A-G

36840549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111213746-A-G

36840606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111213679-T-G

http://identifiers.org/hco/3/GRCh38#36840739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111213562-C-A

http://identifiers.org/hco/3/GRCh38#36840997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111213288-C-A

http://identifiers.org/hco/3/GRCh38#36841066-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111213220-A-C

36841401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111212921-C-T

36841492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111212831-C-G

36841548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111212777-G-A

36841548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111212777-G-C

36841548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111212777-G-T

36842415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111212434-A-G

http://identifiers.org/hco/3/GRCh38#36842472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111212376-C-A

36842472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111212376-C-T

36842603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111212258-T-A

36842603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111212258-T-G

http://identifiers.org/hco/3/GRCh38#36842610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111212240-C-A

36842610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111212240-C-T

36842804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111212058-T-C

36842852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111212014-T-C

36842964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111211876-G-A

36842968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111211872-C-T

36843089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111211744-G-A

36843310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111211574-T-C

36843840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111210380-C-G

36844087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111210187-G-A

36844552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111210070-G-A

36844801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111209797-A-T

36844815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111209783-G-A

36845262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111209389-T-C

36845281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111209373-G-C

36845312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111209350-G-A

36845753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111208513-T-C

36846040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111208320-T-C

http://identifiers.org/hco/3/GRCh38#36846178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111208100-C-A

36846201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111208077-G-A

36846201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111208077-G-T

36846220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111208059-A-G

36846361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111207919-C-T

36846436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111207844-G-T

http://identifiers.org/hco/3/GRCh38#36846437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111207843-C-A

36846437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111207843-C-G

36846869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111207283-T-C

36847017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111207158-C-G

http://identifiers.org/hco/3/GRCh38#36847081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111207113-C-A

36847081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111207113-C-T

http://identifiers.org/hco/3/GRCh38#36847092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111207102-A-C

http://identifiers.org/hco/3/GRCh38#36847231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111206956-C-A

36847231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111206956-C-T

36847444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111206751-A-G

36847541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111206651-G-A

36847948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111206266-C-T

36848089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111206031-T-C

36848490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111205556-T-C

36848740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111205284-G-A

36848896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111205156-G-T

36848936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111205117-T-C

http://identifiers.org/hco/3/GRCh38#36849354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111204765-C-A

36849354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111204765-C-T

36849498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111204631-C-T

36849851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111204295-C-G

36849912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111204233-A-G

36849919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111204226-G-C

36849919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111204226-G-T

36850770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 111203522-A-G

36850798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 111203492-C-T

36850846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 111203445-A-G

36850850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 111203441-T-C

36851083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 111203212-A-G

36851148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 111203148-T-C

36851174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 111203124-T-A

36851174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 111203124-T-C

http://identifiers.org/hco/3/GRCh38#36851215-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111203086-A-C

36851215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 111203086-A-G

http://identifiers.org/hco/3/GRCh38#36851237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111203065-A-C

36851237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 111203065-A-G

http://identifiers.org/hco/3/GRCh38#36851274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111203028-C-A

36851274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 111203028-C-T

36851290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 111203013-T-G

36851370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 111202940-G-A

36851370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 111202940-G-T

36851579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111202734-A-G

36851892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111202433-G-C

http://identifiers.org/hco/3/GRCh38#36851960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111202367-C-A

36851960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111202367-C-G

36851960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111202367-C-T

36852083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111202276-C-T

36852458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111201274-T-A

36852458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111201274-T-C

36852820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111201009-C-T

36852838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111200993-A-T

36852917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111200911-C-G

36852917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111200911-C-T

36853102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111200730-T-A

36853202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111200647-A-T

http://identifiers.org/hco/3/GRCh38#36853334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111200507-C-A

36853504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111200347-C-T

36853791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111200010-T-C

36855274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 111196513-G-A

36855274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 111196513-G-C

http://identifiers.org/hco/3/GRCh38#36855673-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111196114-A-C

36855673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 111196114-A-G

36855838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 111195949-G-A

36856105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 111195682-T-A

36856105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 111195682-T-G

36856177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 111195610-T-C

http://identifiers.org/hco/3/GRCh38#36856197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111195590-A-C

36856197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 111195590-A-G

36856678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 111195115-G-A

36856693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 111195100-T-C

http://identifiers.org/hco/3/GRCh38#36856708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111195085-C-A

36856708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 111195085-C-T

36857323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 111194470-A-G

36857323-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 111194470-A-T

36857331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 111194462-G-C

36857365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 111194431-A-G

36857368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 111194407-T-A

36857368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 111194407-T-C

36857391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 111194384-A-G

36857391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 111194384-A-T

36857429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 111194343-C-T

36857636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 111194154-T-C

36857734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 111194056-T-A

36857734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 111194056-T-C

36857797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 111193993-A-G

36857824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 111193966-T-C

36857899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 111193891-T-C

36857926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 111193864-A-T

36858058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111193732-C-G

36858058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111193732-C-T

36858092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111193698-T-A

36858092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111193698-T-G

36858097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111193693-G-A

36858097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111193693-G-T

36858126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111193681-G-C

36858126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111193681-G-T

http://identifiers.org/hco/3/GRCh38#36858172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111193627-C-A

36858592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111193297-T-C

36858605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111193285-G-A

36858605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111193285-G-T

http://identifiers.org/hco/3/GRCh38#36858607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111193283-C-A

36858607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111193283-C-T

36858747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 111193158-G-T

36858989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111192927-A-T

36858997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111192918-T-A

36858997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111192918-T-C

36859034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111192887-A-G

36859083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111192845-C-T

36859188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111192743-G-A

36859224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111192704-A-G

36859556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111192648-T-G

36859923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111192338-G-C

36859923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111192338-G-T

36860227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111192171-T-C

36860258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111192141-T-A

36860258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111192141-T-C

36860501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111191905-G-A

36860538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111191868-A-G

36860634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111191772-A-G

36860782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111191672-G-A

36860782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111191672-G-C

36860840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111191623-G-A

36861180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111191304-G-C

36861229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111191254-A-G

http://identifiers.org/hco/3/GRCh38#36861325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111191115-C-A

36861325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111191115-C-G

36861512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111190950-C-T

36861550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111190912-C-T

36862553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111189253-G-A

http://identifiers.org/hco/3/GRCh38#36862610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111189216-C-A

http://identifiers.org/hco/3/GRCh38#36862687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111189145-C-A

36862896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111188971-G-A

36863205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111188873-G-A

36863269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111188811-C-T

http://identifiers.org/hco/3/GRCh38#36863308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111188773-A-C

36863901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111187184-T-C

36863926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111187160-T-C

36864017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111187074-C-T

http://identifiers.org/hco/3/GRCh38#36867256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111186725-A-C

36867339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111186633-A-G

36868434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111186127-A-G

36869163-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111185491-A-T

36869190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111185466-T-C

36869273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111185400-G-A

36869374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111185305-A-T

http://identifiers.org/hco/3/GRCh38#36869384-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111185295-A-C

36869489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111185186-T-C

36869511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111185156-G-C

36869526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111185095-C-T

36869533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111185082-G-A

36869628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111184989-C-T

http://identifiers.org/hco/3/GRCh38#36870017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111184653-C-A

36870525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111184507-T-C

36871291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111183976-G-T

36871628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111183725-T-C

36871680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111183673-G-C

36871680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111183673-G-T

36871775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111183558-A-T

36871936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111183234-C-G

36871936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111183234-C-T

36871955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111183215-G-A

36872046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111183143-A-G

36872046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111183143-A-T

36872507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111182769-A-G

36873020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111182306-G-A

http://identifiers.org/hco/3/GRCh38#36873098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111182229-A-C

36873415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111181941-G-A

http://identifiers.org/hco/3/GRCh38#36873875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111181528-C-A

36874146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 111181290-G-A

36874358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111181078-G-T

36874984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111180432-G-A

http://identifiers.org/hco/3/GRCh38#36875002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111180359-C-A

http://identifiers.org/hco/3/GRCh38#36875008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111180353-C-A

36875353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111179997-A-T

36875601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111179747-A-G

36875674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111179656-A-G

36875734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111179609-G-T

36875738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111179605-T-C

36889248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111178990-T-G

http://identifiers.org/hco/3/GRCh38#36889542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111178691-C-A

http://identifiers.org/hco/3/GRCh38#36889800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111178499-C-A

36889800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111178499-C-T

36891863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 111177223-C-T

36892024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111177106-G-A

36892041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111177092-C-T

http://identifiers.org/hco/3/GRCh38#36893019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111176496-A-C

36893019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111176496-A-G

36893107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111176421-T-A

36894085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111176022-G-A

36894138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111175969-T-C

36895048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111175595-T-C

36895054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111175589-G-T

36895617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111174601-G-A

36895617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111174601-G-T

36895618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111174600-A-G

36895863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111174365-A-G

36896183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111174078-G-A

36896183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111174078-G-T

36896542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111173724-T-C

36897524-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111173206-T-A

36898075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111172773-T-C

36898878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111172513-A-G

36898919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111172479-T-C

http://identifiers.org/hco/3/GRCh38#36898959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111172439-C-A

36899029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111172372-C-G

36899029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111172372-C-T

36899243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 111172177-C-G

36899243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 111172177-C-T

36899280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111172142-A-G

36899288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111172134-A-G

http://identifiers.org/hco/3/GRCh38#36900903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111165101-C-A

36901131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111164865-G-T

36901140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111164856-A-T

36901318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111164687-C-G

http://identifiers.org/hco/3/GRCh38#36901343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111164675-C-A

http://identifiers.org/hco/3/GRCh38#36901398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111164623-C-A

36901449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111164587-T-C

36901566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111164324-T-C

36901620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111164278-T-C

36901825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111164122-G-C

36901846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111164109-G-A

36901846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111164109-G-C

36902277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111163896-G-A

36902554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111163377-A-G

36902891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111163057-G-A

36902941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111163007-T-G

36902997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111162952-G-T

36903042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111162901-C-T

http://identifiers.org/hco/3/GRCh38#36903251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111162788-C-A

36903300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111162733-T-C

36903331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111162707-T-C

http://identifiers.org/hco/3/GRCh38#36903431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111162610-C-A

36903431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111162610-C-T

36903435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111162606-C-T

http://identifiers.org/hco/3/GRCh38#36903478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111162566-A-C

36903766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111162297-G-A

36908098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 111161019-G-A

36908214-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111160899-A-T

36908327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 111160796-A-G

36908417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 111160705-A-G

36908502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 111160614-T-C

36908527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 111160590-G-A

36908533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, splice_acceptor_variant, undefined
orthologous variants: 111160584-T-C

http://identifiers.org/hco/3/GRCh38#36908591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#111160527-C-A

36908591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 111160527-C-T

36908652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111160477-T-C

36908730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111160412-G-A

36908730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111160412-G-C

36908981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111160213-G-T

36909037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111160149-C-T

36909093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111160103-C-G

36909242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111159989-T-C

36909359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111159873-G-C

36909981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111159283-A-G

36911211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111158869-C-G

36911358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111158726-A-G

36919708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111157314-A-T

36919820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111157206-T-C

36919962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111157009-A-G

36920340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111156636-G-A

36920534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111156458-A-T

http://identifiers.org/hco/3/GRCh38#36921590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111155647-A-C

36921763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111155458-G-A

36927938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111154664-A-G

http://identifiers.org/hco/3/GRCh38#36928189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111154411-C-A

36928189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111154411-C-T

36928194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111154406-G-T

36928271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111154300-G-A

36929679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111153072-C-T

36929691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111153056-A-G

36932683-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111150692-T-G

36940622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111149527-A-G

36940622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111149527-A-T

36940644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111149505-A-G

36940690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111149465-C-T

36940781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111149379-G-T

36940878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111149284-G-T

36941328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111148299-C-T

36941713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111148018-G-A

36941864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111147828-G-C

36941894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111147808-A-G

36941895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111147807-G-T

36942040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111147478-T-C

36942209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111147315-T-C

36943751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111142124-C-T

http://identifiers.org/hco/3/GRCh38#36943789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111142078-C-A

36943898-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111141968-T-A

36944052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111141821-C-T

36944326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111141631-C-T

36944464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111141522-T-A

36944467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111141519-G-A

36944509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111141496-G-T

http://identifiers.org/hco/3/GRCh38#36944697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111141395-C-A

36944697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111141395-C-T

36944735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111141371-G-A

36944735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111141371-G-T

http://identifiers.org/hco/3/GRCh38#36944762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111141344-C-A

36944762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111141344-C-T

36944763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 111141343-A-G

http://identifiers.org/hco/3/GRCh38#36944767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111141339-C-A

http://identifiers.org/hco/3/GRCh38#36944804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111141300-C-A

36944804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 111141300-C-G

36944804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 111141300-C-T

http://identifiers.org/hco/3/GRCh38#36944838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111141282-C-A

http://identifiers.org/hco/3/GRCh38#36945103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111141111-C-A

36945491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: missense variant
orthologous variants: 111140820-G-A

36945491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29011
most severe consequence: missense variant
orthologous variants: 111140820-G-C