142111798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 40755680-A-G

142111862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40755717-T-C

http://identifiers.org/hco/7/GRCh38#142111892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40755754-C-A

142111892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40755754-C-T

142111908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40755770-A-G

142111928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40755790-G-T

142111952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40755812-A-G

142112028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40755894-G-T

142112157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40756014-A-G

142112209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40756058-G-A

142112226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40756075-G-C

142112252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40756105-C-T

142112625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40756536-C-T

142112701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40756567-C-T

142113171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40757370-A-T

142113214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40757413-C-T

142113316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40757509-G-A

142113422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40757608-G-A

142113612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40757773-G-A

142113684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40757852-G-C

142113745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40757913-G-A

142113794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40757962-G-A

http://identifiers.org/hco/7/GRCh38#142113815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40757981-C-A

142113826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40757992-G-A

142115382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40759123-C-G

142115495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40759217-T-C

http://identifiers.org/hco/7/GRCh38#142116041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40762807-A-C

142116041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40762807-A-G

142116146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40762912-A-G

http://identifiers.org/hco/7/GRCh38#142116176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40762939-A-C

142116209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40762972-C-T

142116356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40763118-G-A

142116777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40763651-T-G

142116784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40763704-A-G

142116831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40763832-G-C

142116945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40763946-C-G

142117178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40764159-T-C

142117184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40764165-C-T

142117198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40764179-T-G

142117336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40764305-G-C

142117547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40764783-C-T

142117609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40764841-A-G

142117665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40764897-T-C

142117738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40764966-A-G

142117814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40765030-T-A

http://identifiers.org/hco/7/GRCh38#142117876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40765086-C-A

142117886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40765096-C-T

142117894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40765104-A-G

http://identifiers.org/hco/7/GRCh38#142117909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40765119-C-A

http://identifiers.org/hco/7/GRCh38#142117929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40765144-C-A

142117929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40765144-C-T

142117930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40765145-T-C

142117966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40765188-T-G

142118451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40766092-A-T

142118499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40766139-C-T

142118657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40766293-C-T

http://identifiers.org/hco/7/GRCh38#142118682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40766371-C-A

http://identifiers.org/hco/7/GRCh38#142118784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40766546-C-A

142118962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40766729-G-T

142119002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40766770-A-G

142119039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40766799-G-A

142119289-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40767708-A-T

142119502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40767885-A-G

142119704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40768055-A-G

http://identifiers.org/hco/7/GRCh38#142119824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40768144-C-A

142120164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40768392-T-C

142120209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40768434-G-C

http://identifiers.org/hco/7/GRCh38#142120253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40768455-C-A

142120253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40768455-C-T

142120285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40768486-C-T

142120425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40768621-T-C

142120425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40768621-T-G

142120497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40768693-A-G

http://identifiers.org/hco/7/GRCh38#142120527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40768717-C-A

142120527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40768717-C-T

142120661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40768827-G-T

142120906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40769018-C-T

142121074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40769192-G-A

142121562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40769521-G-A

142121562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40769521-G-T

142125158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40771707-A-T

142125215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40771762-G-C

142125719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40772436-G-C

142125826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40772537-A-G

142125833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40772544-C-G

142125837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40772548-A-G

142125886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40772593-C-T

142125889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40772596-A-G

142130485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40772765-C-T

142130517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40772805-C-T

http://identifiers.org/hco/7/GRCh38#142130542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40772830-C-A

http://identifiers.org/hco/7/GRCh38#142130666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40772944-A-C

142130667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40772945-A-G

http://identifiers.org/hco/7/GRCh38#142130925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40773202-C-A

142130945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 40773222-C-T

142130951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40773228-A-G

142131041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40773318-G-T

142131057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40773334-C-T

142131813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40773750-G-A

142131813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40773750-G-C

142131885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40773821-G-A

142131984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40773919-G-C

142131984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40773919-G-T

142132002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40773937-T-C

http://identifiers.org/hco/7/GRCh38#142132023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/6/GRCm39#40773958-C-A

142132023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40773958-C-T

142132197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40774110-A-G

142132226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40774143-T-C

142132227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40774144-A-G

142133452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40774352-G-A

142133643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40774469-G-A

142133751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40774532-T-C

142133946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40774725-T-C

http://identifiers.org/hco/7/GRCh38#142134005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40774781-C-A

142134005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40774781-C-T

142134029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40774805-A-T

http://identifiers.org/hco/7/GRCh38#142134095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40774871-C-A

142134095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40774871-C-G

142134095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40774871-C-T

142134150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 40774926-G-A

142134150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, stop_gained
orthologous variants: 40774926-G-T

142134155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40774931-G-T

142134161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40774943-G-A

142134161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40774943-G-T

http://identifiers.org/hco/7/GRCh38#142134162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40774944-C-A

142134162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40774944-C-G

142134162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40774944-C-T

142134172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40774954-G-A

http://identifiers.org/hco/7/GRCh38#142134176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40774958-A-C

142134176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40774958-A-G

142134237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40775021-A-G

142134258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40775042-A-T

142134279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40775063-T-G

142134286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40775070-T-C

142134295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40775079-A-G

http://identifiers.org/hco/7/GRCh38#142134302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40775086-C-A

http://identifiers.org/hco/7/GRCh38#142136506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40776105-A-C

142136506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40776105-A-G

142136524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40776127-T-C

142136537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 40776140-A-G

http://identifiers.org/hco/7/GRCh38#142136588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40776191-A-C

142136588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40776191-A-G

142136597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40776200-G-C

142136597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40776200-G-T

142136627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40776230-C-T

142136754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40776528-A-G

142136833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40776648-T-C

142136931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40776760-G-A

142136961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40776788-T-C

142136974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40776800-G-C

http://identifiers.org/hco/7/GRCh38#142137012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40776828-C-A

142137020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40776836-A-G

142137611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40777393-T-A

142137611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40777393-T-C

142137622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40777399-T-C

142138378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40779163-G-A

142138533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40779353-T-C

http://identifiers.org/hco/7/GRCh38#142138702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40779522-C-A

142138702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40779522-C-T

142138981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40779783-G-A

142138981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40779783-G-T

142139333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40780094-G-A

142139699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40780146-T-G

142139827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40780243-T-C

142139982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40780628-T-C

http://identifiers.org/hco/7/GRCh38#142140003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40780649-C-A

142140165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40780753-C-T

142140357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40780935-A-G

142140700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40781250-A-G

142140761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40781311-T-C

http://identifiers.org/hco/7/GRCh38#142140958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40781513-A-C

142140958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40781513-A-T

142141006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40781563-G-A

142141006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40781563-G-T

142141058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40781618-A-G

http://identifiers.org/hco/7/GRCh38#142141104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40781664-C-A

142141142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40781702-G-A

142141269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40781816-A-G

142141269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40781816-A-T

http://identifiers.org/hco/7/GRCh38#142141475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40782005-C-A

142141500-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40782016-T-A

http://identifiers.org/hco/7/GRCh38#142142192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40782402-A-C

142142192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40782402-A-G

142142279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40782486-C-T

142142411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40782591-A-G

142142440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40782619-A-G

142143135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40783139-T-C

142143137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40783141-T-C

142143159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40783163-T-C

142143166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40783170-A-G

142143503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40790100-A-G

142143616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40790210-T-A

142143619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40790213-G-A

142143619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40790213-G-T

http://identifiers.org/hco/7/GRCh38#142143727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40790325-C-A

142143728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40790326-T-C

142143856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40790457-C-T

http://identifiers.org/hco/7/GRCh38#142143929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40790529-C-A

142143929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40790529-C-T

142143947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40790547-T-G

142144114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40790677-G-T

http://identifiers.org/hco/7/GRCh38#142144121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40790684-C-A

142144121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40790684-C-T

142144191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40790768-T-C

142144826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40791243-G-A

142144826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40791243-G-T

142144881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40791297-C-T

142144968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40791382-T-C

142144969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40791383-G-A

142145881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40791490-T-C

142145995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40791619-T-C

http://identifiers.org/hco/7/GRCh38#142146072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40791702-C-A

142146201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40791814-G-A

142146201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40791814-G-T

142146236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40791846-A-T

142146466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40792148-G-A

142146474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40792156-A-G

142146578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40792250-C-T

142146584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40792256-A-G

142147059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40792395-A-G

142147110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40792446-C-T

142147129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40792465-T-G

142147271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40792552-T-C

http://identifiers.org/hco/7/GRCh38#142147328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40792605-C-A

142147336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40792613-G-A

http://identifiers.org/hco/7/GRCh38#142147344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40792621-C-A

142147379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40792650-G-T

142147596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40792864-A-G

142147634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40792914-T-G

142147646-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40792926-T-A

142147686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40792963-A-G

142147686-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40792963-A-T

142147693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40792970-G-A

142148099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40793316-A-G

142148111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40793328-G-A

142148113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40793330-G-A

142148117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40793334-A-G

142151574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40794185-C-G

142151623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40794229-G-A

142151632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40794238-A-G

142151699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40794301-G-T

142151964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40795354-T-A

142151967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40795357-A-G

142152081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40795480-A-G

142152199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40795562-C-T

142152252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40795603-A-G

142153719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40795984-G-T

142153733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40795998-C-T

142153792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40796059-T-G

http://identifiers.org/hco/7/GRCh38#142153798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40796065-C-A

142153873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40796133-A-T

142153906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40796168-C-T

http://identifiers.org/hco/7/GRCh38#142153977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40796239-C-A

http://identifiers.org/hco/7/GRCh38#142154029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40796291-C-A

142154029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40796291-C-T

142154266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40796515-T-C

142154285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40796534-T-A

142154533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40796766-T-C

142154586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40796832-G-A

142154586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40796832-G-C

142154586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40796832-G-T

http://identifiers.org/hco/7/GRCh38#142154596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40796842-C-A

142154596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40796842-C-T

142154604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40796850-C-G

142154604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40796850-C-T

142154844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 40797081-G-A

142154851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40797088-G-A

142154851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40797088-G-T

142154898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40797133-G-T

142154989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40797209-G-A

142154989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40797209-G-T

142155000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40797216-A-G

142155137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40797569-G-A

142155168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40797618-G-A

142155168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40797618-G-C

142155211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40797650-G-A

142155211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40797650-G-T

142155430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40797841-C-T

142155552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40798834-T-A

142155552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40798834-T-C

142156237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40799140-T-C

142156314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40799215-T-A

142156366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40799260-G-A

142156398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40799300-T-C

142156464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40799365-C-T

142156547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40799445-T-C

142156549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40799447-G-A

142156690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40799566-G-A

142156730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40799593-C-T

142156783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40799644-A-G

142156874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40799784-T-C

142157083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40799979-T-G

142157116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40800013-A-G

142157140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40800038-A-G

142157176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40800075-A-G

142157799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40800377-A-G

142157806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40800384-C-G

142157846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40800424-G-A

142157846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40800424-G-C

http://identifiers.org/hco/7/GRCh38#142157933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40800492-C-A

142157959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40800518-G-A

142157959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40800518-G-C

142157961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40800520-G-A

142157962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40800521-T-C

http://identifiers.org/hco/7/GRCh38#142158035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40800594-C-A

142158035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40800594-C-T

142158130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40800685-T-C

142158153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40800707-G-A

142158416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40800954-G-A

142158416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40800954-G-T

142158423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40800961-T-C

142158781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40801254-C-T

142158831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40801298-T-C

142158971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40801378-G-T

142159099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40801498-T-C

142159114-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40801514-T-G

142159142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40801542-G-A

142159147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40801547-T-A

142159182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40801583-A-G

142159211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40801612-G-A

142159249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40801648-G-T

142159283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 40801729-C-G

142159288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 40801734-G-T

142159403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40801827-G-A

142159403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40801827-G-T

142159429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40801850-A-G

142159462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40801884-T-C

142159483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40801899-G-A

142159483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40801899-G-C

142159483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40801899-G-T

142159586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40802003-A-G

http://identifiers.org/hco/7/GRCh38#142160011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40802755-A-C

142160023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40802767-T-C

142160347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40803071-A-G

142160414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40803134-G-T

142160501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40803217-A-G

142160596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40803306-T-C

142160617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40803313-C-T

142160928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40803579-C-G

142160985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40803628-A-T

142161119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 40803773-T-C

142161122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 40803775-C-T

142161182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40803835-G-T

142161217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40803870-G-A

http://identifiers.org/hco/7/GRCh38#142161315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40803965-C-A

142161315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40803965-C-G

142161315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40803965-C-T

142161451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40804102-T-G

142161629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40804288-A-G

http://identifiers.org/hco/7/GRCh38#142161758-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40804418-A-C

142161829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40804489-T-A

142161829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40804489-T-C

142161829-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40804489-T-G

142161832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40804492-A-G

142161952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 40804601-T-C

142163951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40805243-T-C

142164016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40805314-G-T

http://identifiers.org/hco/7/GRCh38#142164126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40805425-C-A

142164163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40805473-A-G

142164226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40805536-A-G

142164226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40805536-A-T

142164281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40805598-C-T

142164475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40805843-A-G

142164511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40805919-A-G

142164527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40805935-G-T

142164537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40805945-G-A

142164537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40805945-G-T

142164675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40806066-A-T

142164680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40806071-A-T

142164826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40806199-T-C

142164919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_acceptor_variant
orthologous variants: 40806292-G-T

142165055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40806427-T-C

142165367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40806721-T-C

142165445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40806809-G-A

142165599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40806988-G-A

142165797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40807214-A-G

142165797-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40807214-A-T

142165823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40807235-C-T

142166034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40807644-C-T

http://identifiers.org/hco/7/GRCh38#142166042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40807652-C-A

142166042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40807652-C-G

142166238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40807848-G-A

142166238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40807848-G-C

142166241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40807851-G-A

142166241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40807851-G-C

142166241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40807851-G-T

142166425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40808043-A-T

142166442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40808060-A-G

http://identifiers.org/hco/7/GRCh38#142167018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40808134-C-A

142167111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40808227-C-T

142167122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40808238-A-T

142167138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40808258-A-G

142167139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40808259-G-T

142167157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40808277-A-G

142167178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40808292-G-A

142167257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40808373-T-C

142167321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40808437-T-C

142167514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40808645-C-T

142168036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40809348-A-G

http://identifiers.org/hco/7/GRCh38#142170041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40809478-C-A

142170041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40809478-C-T

142170066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40809498-T-C

142170247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40809690-G-T

142170283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40809726-A-G

http://identifiers.org/hco/7/GRCh38#142170297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40809740-C-A

142170297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40809740-C-G

142170297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40809740-C-T

142170316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40809759-A-G

142170764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40810058-C-G

142170764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40810058-C-T

http://identifiers.org/hco/7/GRCh38#142170890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40810182-C-A

142170924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40810214-T-C

http://identifiers.org/hco/7/GRCh38#142171063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40810351-C-A

142171063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40810351-C-T

http://identifiers.org/hco/7/GRCh38#142171116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40810405-C-A

142171345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40810730-T-C

142171350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40810735-C-T

142171508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40810896-T-C

142171566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40810953-G-A

142171566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40810953-G-T

142171576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40810963-A-T

142172218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40811796-T-A

142172218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40811796-T-C

142172228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40811806-G-A

142172228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40811806-G-C

142172228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40811806-G-T

142172244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40811822-C-T

142172275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40811855-A-G

142172275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40811855-A-T

http://identifiers.org/hco/7/GRCh38#142172311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40811881-C-A

http://identifiers.org/hco/7/GRCh38#142172505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40812060-C-A

142172505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40812060-C-T

142172548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40813032-G-A

142172548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40813032-G-C

142172548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40813032-G-T

142172589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40813072-G-T

142172602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40813085-G-A

142172602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40813085-G-T

http://identifiers.org/hco/7/GRCh38#142172610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40813093-C-A

142172610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40813093-C-T

http://identifiers.org/hco/7/GRCh38#142172613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40813096-C-A

142172613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40813096-C-G

142172641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40813120-T-C

142172641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40813120-T-G

http://identifiers.org/hco/7/GRCh38#142172698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40813177-A-C

142172698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40813177-A-T

142172783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40813262-C-T

142172927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40813498-A-G

http://identifiers.org/hco/7/GRCh38#142173022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40813600-A-C

142173039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40813617-A-G

142173121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40813687-G-A

142173121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40813687-G-C

142173121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40813687-G-T

142173337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40813993-G-A

142173337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40813993-G-T

http://identifiers.org/hco/7/GRCh38#142173441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40814604-C-A

142173581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40814750-C-T

142173668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40814837-A-G

142173770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40814930-G-A

142175429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40815226-G-C

142175614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40815403-C-T

142175616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40815405-G-A

http://identifiers.org/hco/7/GRCh38#142175624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40815413-C-A

142175624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40815413-C-T

http://identifiers.org/hco/7/GRCh38#142175684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40815474-C-A

142176110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40815876-G-A

142176110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40815876-G-C

142176110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40815876-G-T

142176160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40815925-C-T

142176684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40816692-T-C

142176863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40816861-A-T

142182949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40817331-G-A

142182949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40817331-G-T

http://identifiers.org/hco/7/GRCh38#142183212-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40817559-A-C

142183230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40817577-T-G

142183301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40817646-C-T

http://identifiers.org/hco/7/GRCh38#142183352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40817697-C-A

142183352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40817697-C-T

142183415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40817758-A-G

142183440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40817768-A-G

142183500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40817828-A-T

142183563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40817887-T-C

142183645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40817970-C-T

142183829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40818115-T-C

142184345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40818300-T-C

142184399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40818346-T-C

142184415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40818363-G-T

142184548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40818487-G-C

142184780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40818769-G-A

142184914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40818908-C-T

142184959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40818952-G-A

http://identifiers.org/hco/7/GRCh38#142184991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40818981-C-A

142185009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40818999-A-G

142185023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40819013-A-G

142185843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40819723-C-T

142185879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40819759-G-C

142185911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40819789-A-G

http://identifiers.org/hco/7/GRCh38#142185916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40819794-C-A

142185916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40819794-C-T

142185964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40819854-A-G

142186024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40819914-T-C

142186024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40819914-T-G

142186087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40819977-G-A

142186087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40819977-G-T

142186118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40820008-T-A

142186169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40820046-G-A

142186169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40820046-G-T

http://identifiers.org/hco/7/GRCh38#142186739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40820528-C-A

142186753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40820542-G-A

142186762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40820551-G-A

142186815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40820607-C-T

142186930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40820719-T-C

142187187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40821179-G-C

142187187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40821179-G-T

http://identifiers.org/hco/7/GRCh38#142187279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40821237-A-C

142187522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40821458-C-T

142187629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40821523-T-C

142187737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40821611-T-C

142187799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40821673-G-A

142187803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40821677-T-C

142187862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40821716-T-C

142187917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40821758-A-G

142187944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40821800-A-G

142187976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40821833-G-T

142188019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40821876-A-G

142188059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40821906-A-T

142188188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40822009-T-C

142189159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40822505-T-C

http://identifiers.org/hco/7/GRCh38#142189238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40822580-C-A

142189321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40822615-T-A

142189321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40822615-T-C

http://identifiers.org/hco/7/GRCh38#142189383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40822678-C-A

142189383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40822678-C-T

142189493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40822788-G-A

142189493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40822788-G-C

142189493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40822788-G-T

142189516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40822811-T-C

142192558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40827692-G-A

142192561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40827695-G-C

142192561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40827695-G-T

http://identifiers.org/hco/7/GRCh38#142192726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40827851-C-A

http://identifiers.org/hco/7/GRCh38#142193236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40828980-C-A

142194896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40829448-A-T

http://identifiers.org/hco/7/GRCh38#142195026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40829568-A-C

142195801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830196-G-A

http://identifiers.org/hco/7/GRCh38#142196055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40830406-C-A

142196055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830406-C-T

http://identifiers.org/hco/7/GRCh38#142196151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40830502-C-A

142196151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 40830502-C-T

http://identifiers.org/hco/7/GRCh38#142196187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40830538-C-A

142196187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40830538-C-T

142196208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40830559-T-C

142196327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830677-G-A

142196377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830718-A-G

142196377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830718-A-T

142196389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830730-G-A

142196389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830730-G-T

142196405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830746-A-T

142196408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830749-G-C

http://identifiers.org/hco/7/GRCh38#142196497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40830829-C-A

142196527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830859-G-A

142196527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830859-G-C

142196527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830859-G-T

http://identifiers.org/hco/7/GRCh38#142196528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40830860-C-A

142196528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830860-C-T

142196548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830881-G-A

142196548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830881-G-C

142196548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830881-G-T

142196558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 40830891-T-C

http://identifiers.org/hco/7/GRCh38#142196566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40830899-C-A

142196566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 40830899-C-T

http://identifiers.org/hco/7/GRCh38#142196807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40831123-C-A

142196807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40831123-C-T

http://identifiers.org/hco/7/GRCh38#142196835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40831154-C-A

142196835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40831154-C-T

http://identifiers.org/hco/7/GRCh38#142196877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40831199-C-A

http://identifiers.org/hco/7/GRCh38#142196922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40831705-C-A

142196928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40831711-A-T

142196953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40831736-A-G

142196988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40831771-G-A

142197122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40831899-C-T

142197201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40832000-A-T

142197247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40832050-G-A

142197296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40832099-G-A

142197296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40832099-G-T

142197311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40832114-T-A

142197311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40832114-T-C

142197311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40832114-T-G

http://identifiers.org/hco/7/GRCh38#142197338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40832145-C-A

http://identifiers.org/hco/7/GRCh38#142197347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40832154-C-A

142197616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40832422-G-A

142197742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40832548-T-C

142197747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40832553-G-A

142198241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40833250-G-A

142198273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40833279-G-A

142198273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40833279-G-T

142198291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40833297-A-G

142198304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40833311-T-A

142198403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40833392-C-T

142198515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40833495-T-C

142198555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40833533-A-G

http://identifiers.org/hco/7/GRCh38#142198650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40833629-C-A

142198650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40833629-C-T

142198668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40833647-C-T

142198749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40833725-A-G

142198855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40833806-A-G

142199015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40833962-T-A

142199645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40834408-T-C

http://identifiers.org/hco/7/GRCh38#142199822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40834587-C-A

142199822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40834587-C-T

142199823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40834588-T-G

http://identifiers.org/hco/7/GRCh38#142200019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40834779-C-A

142200019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40834779-C-T

142200042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40834819-A-G

142208479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40835984-C-G

142208523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40836024-C-T

142208628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40836130-A-T

http://identifiers.org/hco/7/GRCh38#142208657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40836158-C-A

142208679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40836180-A-G

142208679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40836180-A-T

http://identifiers.org/hco/7/GRCh38#142208728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40836223-C-A

142208728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40836223-C-T

142208759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40836252-G-A

142208759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40836252-G-T

142208932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40836428-A-G

142208959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40836455-T-G

142209043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40836550-A-T

142209102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40836597-G-T

142218220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40841725-A-G

142218505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40842005-A-G

http://identifiers.org/hco/7/GRCh38#142218510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40842010-C-A

142218523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40842023-T-C

142218626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40842099-G-T

142218738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40842205-A-G

142218890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40842345-C-T

142219102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40842572-A-G

142219111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40842581-A-G

http://identifiers.org/hco/7/GRCh38#142219314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40842789-C-A

142219375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40842857-G-T

142219499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40842977-A-G

142219671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40843154-G-A

142219960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40843431-C-G

142219993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40843464-C-T

142220119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40843755-A-G

142220122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40843758-G-A

142220158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40843794-C-G

142220158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40843794-C-T

142220164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40843800-C-T

142220203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40843839-C-G

142220225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40843861-C-G

142220293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40843929-G-A

http://identifiers.org/hco/7/GRCh38#142220317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40843953-A-C

142220317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40843953-A-G

142220338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40843974-T-C

142220420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40844056-C-G

142220458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40844094-C-G

142220479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40844115-A-G

http://identifiers.org/hco/7/GRCh38#142220523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40844159-C-A

http://identifiers.org/hco/7/GRCh38#142220530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40844166-A-C

142220893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40844526-G-T

142220911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40844544-A-G

142220968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40844601-A-G

142221031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40844664-C-T

142221061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40844694-C-G

142221061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40844694-C-T

142221161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40844803-T-C

142221262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40844904-A-T

142221278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40844920-C-T

142221282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40844924-A-G

142221292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense variant
orthologous variants: 40844934-T-A

142221346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense variant
orthologous variants: 40845015-A-G

http://identifiers.org/hco/7/GRCh38#142221355-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40845024-A-C

142221369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: synonymous variant
orthologous variants: 40845038-T-C

http://identifiers.org/hco/7/GRCh38#142221543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40845250-C-A

142221543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: synonymous variant
orthologous variants: 40845250-C-T

142221548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense variant
orthologous variants: 40845255-T-G

142221576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: synonymous variant
orthologous variants: 40845283-T-C

142221599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense variant
orthologous variants: 40845306-C-T

142221757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense variant
orthologous variants: 40846018-A-G

http://identifiers.org/hco/7/GRCh38#142221862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40846142-C-A

http://identifiers.org/hco/7/GRCh38#142221979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#40846241-A-C

142221979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28101
most severe consequence: missense variant
orthologous variants: 40846241-A-T