87453197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111701967-C-G

87453197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111701967-C-T

87453257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111702028-A-G

87453274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111702045-C-T

87453514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111702283-C-T

87453558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111702327-T-A

87453558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111702327-T-G

87453745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111702511-T-C

87453752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111702518-G-T

87453790-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111702557-A-T

87453851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111702608-T-C

http://identifiers.org/hco/13/GRCh38#87453860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111702617-C-A

87453867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111702624-A-G

87453904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111702661-A-T

87454133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111702791-A-G

87454178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111702834-C-T

87454209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111702864-G-T

87454416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111703077-C-T

87454435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111703094-G-A

http://identifiers.org/hco/13/GRCh38#87454711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111703296-C-A

87454711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111703296-C-T

87454714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111703299-C-G

87460128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111706043-C-T

87460136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111706051-G-A

87460181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111706091-G-A

87460181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111706091-G-T

87460401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111706309-G-A

87460601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111706491-G-A

87460601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111706491-G-T

87460680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111706554-T-G

87460789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111706636-C-T

87460863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111706690-T-C

http://identifiers.org/hco/13/GRCh38#87461001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111706769-A-C

87461231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111707114-G-A

87461231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111707114-G-T

87461252-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111707128-T-A

87461313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111707189-T-G

87461640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111707597-G-A

87461641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111707598-G-C

87461641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111707598-G-T

87461698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111707640-T-A

87461748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111707659-T-C

87461761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111707672-C-T

87462326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111708234-G-A

87462326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111708234-G-C

87462326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111708234-G-T

87462371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111708302-A-T

87462508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111708435-A-G

http://identifiers.org/hco/13/GRCh38#87462632-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111708540-A-C

87462769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111708669-C-T

87462844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111708852-T-G

87463030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111709082-G-A

87476591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111713831-T-C

87476719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111713959-A-G

87476930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111714143-C-T

87477293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111714403-T-C

87477315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111714451-A-G

87477321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111714457-C-G

87477321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111714457-C-T

http://identifiers.org/hco/13/GRCh38#87495884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111721912-C-A

87496061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111722068-T-A

87496061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111722068-T-C

87496140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111722144-G-A

87496285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111722286-C-T

87496549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111722543-T-A

87496626-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111722589-A-T

87496729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111722688-T-C

87497121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111722757-G-A

87497211-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111722845-T-G

http://identifiers.org/hco/13/GRCh38#87498213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111723805-C-A

http://identifiers.org/hco/13/GRCh38#87498360-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111723952-A-C

http://identifiers.org/hco/13/GRCh38#87498464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111724055-C-A

87498464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111724055-C-T

87498504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111724095-T-C

87498586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111724169-A-G

87498964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111724528-A-G

87498964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111724528-A-T

http://identifiers.org/hco/13/GRCh38#87498976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111724540-A-C

87499211-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111724756-T-G

87499318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111724858-T-A

87499338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111724876-T-C

87499387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111724924-G-T

87499603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111725221-T-A

87499603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111725221-T-C

87501824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111745259-A-G

87501880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111745314-G-A

87501905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111745338-A-G

87501928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111745352-G-T

http://identifiers.org/hco/13/GRCh38#87508993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111747764-C-A

87508993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111747764-C-G

87508999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111747770-C-T

87509039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111747816-A-T

87509113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111747862-T-G

87509125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111747874-T-C

87509138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111747887-A-G

87509138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111747887-A-T

87509266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111748007-C-T

87509397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111748138-T-G

87509435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111748176-C-T

87509457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111748198-G-A

87509529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111748271-G-A

87509542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111748282-G-A

87509620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111748360-T-A

87509620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111748360-T-C

87509853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111748584-G-T

87510147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111748889-G-A

87510283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111749025-T-C

http://identifiers.org/hco/13/GRCh38#87511570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111751084-C-A

87511982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111752888-G-C

87512114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111753021-T-C

87512159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111753058-T-C

87512191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111753083-T-C

87512317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111753197-G-A

87512352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111753238-G-A

87512352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111753238-G-C

87512373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111753259-A-G

87512682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111753554-G-C

87512908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111753755-T-C

87512942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111753801-T-C

87513326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111754161-T-A

87513401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111754239-G-T

87513537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111754405-T-C

87513547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111754415-G-C

87513547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111754415-G-T

http://identifiers.org/hco/13/GRCh38#87513586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111754464-A-C

87513597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111754472-G-C

87513665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111754541-C-T

http://identifiers.org/hco/13/GRCh38#87514481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111754794-A-C

87514482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111754795-A-T

87514663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111754963-T-C

87514715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111755002-C-T

87514748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111755032-G-A

87514849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111755111-A-G

87514870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111755123-G-C

87514879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111755132-A-G

87514975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111755227-T-C

87519049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111756738-A-G

87519064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111756744-T-C

87519254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111756953-C-T

87519285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111756984-A-G

87519551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111757234-A-G

87519583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111757263-C-T

87519645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111757325-C-T

87519682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111757351-G-T

87519765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111757414-C-T

87523758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111757714-A-G

87523779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111757735-A-G

87524047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111758033-T-C

87524094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111758086-G-C

87524118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111758110-T-A

87524133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111758125-T-G

87525004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111760524-G-A

87525004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111760524-G-C

http://identifiers.org/hco/13/GRCh38#87525022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111760542-C-A

87525022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111760542-C-T

87525228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111760727-A-G

87525245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111760744-A-G

87525518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111761145-G-C

87525688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111761296-A-T

87525782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111761387-G-A

87526203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111762766-T-C

87526381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111762977-G-A

87526422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111763022-C-T

87526505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111763089-T-C

http://identifiers.org/hco/13/GRCh38#87526622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111763203-C-A

87526623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111763204-T-C

87526778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111763346-T-C

87526800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111763373-T-C

87526967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111763515-C-T

87526970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111763518-T-C

87527013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111763575-T-C

87527414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111765661-T-C

87528238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111766091-T-C

87528248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111766100-A-G

87528248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111766100-A-T

87528278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111766130-A-G

87528563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111766778-A-G

87528589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111766809-T-C

http://identifiers.org/hco/13/GRCh38#87528610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111766828-C-A

87528677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111766889-G-C

87528677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111766889-G-T

87542675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111775509-T-C

http://identifiers.org/hco/13/GRCh38#87542904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111775697-C-A

87543028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111775802-G-C

87543063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111775837-A-G

87543066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111775844-C-T

87547207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111779239-C-T

87549167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111785508-A-G

87549300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111785626-C-T

http://identifiers.org/hco/13/GRCh38#87549387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111785726-C-A

87549387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111785726-C-T

87549418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111785790-G-T

87549475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111785844-A-G

87549475-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111785844-A-T

87549489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111785858-C-T

87549534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111785903-G-A

87549543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111785912-C-T

87549662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111786026-C-T

87549729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111786086-T-A

87549729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111786086-T-C

87549729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111786086-T-G

87549787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111786113-A-G

87549789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111786115-T-A

87549924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111786247-G-C

87549929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111786252-T-C

87549995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111786318-T-C

http://identifiers.org/hco/13/GRCh38#87549998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111786321-C-A

87550043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111786359-C-T

87550394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111786692-A-G

87550507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111786761-G-T

http://identifiers.org/hco/13/GRCh38#87550577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111786828-C-A

87550614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111786863-C-T

87571048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111821921-G-C

87571153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111822015-G-C

87571237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111822105-A-G

87571240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111822108-T-A

87571264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111822132-G-A

87571264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111822132-G-C

87571264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111822132-G-T

87571412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111822266-T-A

87571413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111822267-G-A

87571459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111822311-C-T

87571563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111822410-T-C

87571668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111822518-C-T

87571804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111822677-T-C

87571852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111822827-C-G

87572050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111823087-A-T

87572114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111823147-A-G

87572191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111823319-C-T

87572231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111823430-G-C

87572231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111823430-G-T

87572241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111823440-C-T

87572452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111823646-A-G

87572763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111823934-T-A

http://identifiers.org/hco/13/GRCh38#87572807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111823978-C-A

87572807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111823978-C-T

87572838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111824006-G-A

87572858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111824024-T-C

87572911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111824100-A-G

87572927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111824116-G-A

http://identifiers.org/hco/13/GRCh38#87572981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111824165-C-A

87572981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111824165-C-G

87573032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111824221-A-G

87573073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111824252-C-T

87573804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111824904-A-G

87573837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111824947-A-G

87573915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111825041-A-G

87574266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111825853-A-G

87574296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111825882-T-G

87574358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111825936-T-C

http://identifiers.org/hco/13/GRCh38#87574511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111826075-C-A

87574511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111826075-C-T

87574551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111826116-G-A

87574563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111826128-T-A

87574684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111826248-A-T

http://identifiers.org/hco/13/GRCh38#87576688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111829899-C-A

87576977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111830173-A-G

87577029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111830229-G-A

87577029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111830229-G-C

87577029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111830229-G-T

87578960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111835227-G-A

87578960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111835227-G-T

87579129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111835393-C-G

http://identifiers.org/hco/13/GRCh38#87579244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111835416-C-A

87579306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111835469-T-A

http://identifiers.org/hco/13/GRCh38#87579517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111835684-C-A

87588901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111839957-T-A

87589109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111840202-C-G

87589122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111840214-G-A

87589130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111840222-C-T

87589142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111840235-C-T

87589179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111840270-G-A

87589259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111840338-G-T

http://identifiers.org/hco/13/GRCh38#87589293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111840371-C-A

87610625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111845647-G-A

87610674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111845702-T-C

87610674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111845702-T-G

87610797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111845818-T-G

87610842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111845849-T-C

http://identifiers.org/hco/13/GRCh38#87610977-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111845973-A-C

87610977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111845973-A-G

http://identifiers.org/hco/13/GRCh38#87610979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111845975-C-A

87613979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111846800-T-C

87614076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111846894-C-T

87614077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111846895-C-T

87614221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111847037-T-C

87614266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111847075-G-C

87614266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111847075-G-T

87614305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111847117-T-A

87614319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111847131-A-T

87614680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111847214-G-T

87614846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111847595-G-A

87614874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111847622-A-T

87614961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111847687-T-C

87615013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111847738-G-A

87615097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111847862-A-G

87615155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111847916-T-C

87620605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111851910-G-T

87620677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111851981-A-T

http://identifiers.org/hco/13/GRCh38#87620758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111852066-C-A

87620758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111852066-C-G

87620845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111852139-T-C

http://identifiers.org/hco/13/GRCh38#87620928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111852219-C-A

87620949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111852229-T-C

87621017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111852292-G-A

87621052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111852325-T-C

http://identifiers.org/hco/13/GRCh38#87621070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111852356-C-A

87621255-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111852650-A-T

87621472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111852845-T-C

87621552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111852914-A-T

87621703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111853059-A-G

87621757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111853092-T-C

87621859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111853197-A-G

87622150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111853484-A-T

87622318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111853643-A-G

87622372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111853696-G-A

87622378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111853702-T-C

http://identifiers.org/hco/13/GRCh38#87622411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111853742-A-C

87622501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111853819-A-G

87622578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111853884-C-T

87622701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111854003-C-T

87622716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111854018-G-T

87622717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111854019-C-T

87622718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111854020-T-C

87622728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111854030-T-A

87622882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111854155-G-A

87622927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111854199-G-A

87622927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111854199-G-T

87622943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111854211-C-T

87623161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111854420-G-T

87623206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111854462-A-G

87623310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111854563-A-G

http://identifiers.org/hco/13/GRCh38#87623362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111854622-C-A

87623362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111854622-C-T

87623383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111854642-G-A

87623590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111854840-T-C

87623766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111854970-T-C

87623822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111855020-T-C

87623874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111855074-T-A

87623874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111855074-T-G

87623901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111855101-G-T

87623914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111855126-C-T

http://identifiers.org/hco/13/GRCh38#87624002-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111855201-A-C

87624053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111855248-A-G

http://identifiers.org/hco/13/GRCh38#87624159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111855331-C-A

87624386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111855501-C-G

87625055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111855938-T-C

87625112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111855959-G-A

87625112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111855959-G-C

87625243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111856082-G-T

87625365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111856208-A-G

87625419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111856263-G-A

87625647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111856472-G-A

87625781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111856604-T-C

87625787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111856610-T-C

87625806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111856629-C-G

87625806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111856629-C-T

87626331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111856652-A-G

87626501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111856807-G-C

87626866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111857174-G-A

87626894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111857202-T-A

http://identifiers.org/hco/13/GRCh38#87627109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111857376-C-A

http://identifiers.org/hco/13/GRCh38#87627111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111857378-A-C

87627111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111857378-A-G

87627134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111857401-A-G

http://identifiers.org/hco/13/GRCh38#87627175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111857445-A-C

http://identifiers.org/hco/13/GRCh38#87627420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111857687-C-A

87627420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111857687-C-T

http://identifiers.org/hco/13/GRCh38#87627470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111857741-C-A

87627470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111857741-C-G

87628746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111857933-A-G

http://identifiers.org/hco/13/GRCh38#87628820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111857992-A-C

87628820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111857992-A-G

87628971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111858083-G-A

87629070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111858168-C-T

87629324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111858400-G-A

87629451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111858527-T-A

87629555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111858630-A-G

http://identifiers.org/hco/13/GRCh38#87629646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111858690-C-A

87629646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111858690-C-G

87629652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111858696-C-G

87629721-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111858767-T-G

87629768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111858815-A-G

87629792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111858839-T-A

87630164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111859191-G-A

87630314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111859671-G-A

87630389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111859740-T-C

87630525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111860248-A-G

87630659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111860392-T-C

87630880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111860692-A-G

87631022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111860819-G-A

http://identifiers.org/hco/13/GRCh38#87631108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111860902-A-C

87631108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111860902-A-G

http://identifiers.org/hco/13/GRCh38#87631153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111860936-A-C

87631192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111860958-T-C

87631334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111861124-A-G

87632134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111861413-G-C

87632673-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111861782-T-A

87632684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111861793-T-C

87632770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111861864-A-G

87632938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111862069-C-T

87632993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111862127-T-C

87633165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111862284-T-C

87636000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111862330-T-C

87636771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111863066-T-A

87636771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111863066-T-C

87636807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111863104-G-C

87636864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111863153-G-A

87636904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111863195-G-A

87637001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111863259-G-A

87637001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111863259-G-T

87637485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111863427-T-G

87637517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111863457-T-C

http://identifiers.org/hco/13/GRCh38#87637519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111863459-A-C

87637539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111863478-T-G

87637573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111863511-A-T

87637586-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111863524-T-A

87637706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111863794-G-A

87637706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111863794-G-T

87637745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111863833-G-A

87637950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111864010-A-G

87637976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111864036-A-G

87638032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111864091-G-T

87638144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111864205-A-G

87638333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111864472-T-A

87638513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111864631-G-A

87638727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111864819-A-T

87638734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111864826-T-C

87638827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111864918-G-T

87639591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111865060-T-C

87639739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111865196-A-G

87640138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111865603-T-C

87642670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111870737-C-G

87642676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111870743-C-T

http://identifiers.org/hco/13/GRCh38#87642719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111870786-C-A

87642719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111870786-C-T

87642728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111870795-T-C

87642827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111870912-G-T

87642880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111870960-A-G

87642898-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111870978-A-T

http://identifiers.org/hco/13/GRCh38#87643021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111871086-A-C

87644549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111871419-A-G

87644577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111871447-C-T

87647828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111872117-G-A

87647847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111872136-G-A

87647847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111872136-G-C

87648716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111872677-A-T

87648798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111872755-A-G

87648820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111872777-A-G

87648934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111872895-G-C

http://identifiers.org/hco/13/GRCh38#87648967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111872934-C-A

87649201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111873937-A-T

87649264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111874002-T-C

87649270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111874008-T-G

87649277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111874015-G-T

87649397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111874122-A-T

87649490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111874211-G-A

87649490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111874211-G-T

87649607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111874327-G-A

87649683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111874399-G-A

87649734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111874439-G-A

87649820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111874534-G-A

87649845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111874558-T-A

87652563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111877072-T-G

87652755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111877243-C-T

87652783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111877271-G-A

87657704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111883957-T-C

87657715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111883966-C-T

87657871-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111884332-T-A

87657882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111884343-G-A

87657950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111884415-A-T

87659064-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111884812-T-G

87659149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111884890-T-C

87659188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111884929-A-G

87659234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111884975-G-A

87659240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111884981-T-A

87659240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111884981-T-C

87659378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111885117-T-G

87659438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111885180-G-A

87659483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111885225-A-G

87659562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111885287-T-G

87659591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111885323-C-T

87660082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111886202-G-A

87660289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111886410-A-G

87660309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111886446-C-G

87660309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111886446-C-T

87660345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111886485-C-T

87660426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111886557-T-C

87660456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111886621-T-C

87660474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111886656-T-C

87660535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111886887-A-G

87660560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111886912-G-A

87660727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111887075-T-G

87660742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111887090-G-A

87660757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111887104-A-G

87660765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111887112-C-G

87660927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111887278-T-C

87661363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111887713-G-A

87661480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111887827-T-C

87661704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111888051-T-C

87662461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111898518-C-T

87662462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111898519-A-T

87662472-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111898529-T-G

http://identifiers.org/hco/13/GRCh38#87662476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111898534-C-A

87662516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111898574-C-T

87662588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111898652-T-A

http://identifiers.org/hco/13/GRCh38#87662618-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111898682-A-C

87662629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111898693-C-T

87662634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111898697-G-T

87662850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111898927-C-G

87662911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111898996-A-G

87663455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111900164-A-G

87663513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111900220-C-T

87663552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111900259-G-T

87663639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111906782-T-C

87663806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111906944-C-T

87666578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111907653-G-C

87666578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111907653-G-T

87666579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111907654-T-C

87666582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111907657-G-A

http://identifiers.org/hco/13/GRCh38#87666606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111907681-C-A

87666606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111907681-C-G

87666611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111907686-C-G

87666611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111907686-C-T

87666630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111907705-G-A

http://identifiers.org/hco/13/GRCh38#87666703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111907786-A-C

87666728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111907809-T-G

87666796-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111907874-T-A

http://identifiers.org/hco/13/GRCh38#87666813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111907891-C-A

http://identifiers.org/hco/13/GRCh38#87666833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111907903-C-A

87666942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111908012-T-C

87666985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111908054-T-C

87667051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111908117-G-A

87667051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111908117-G-C

87667051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111908117-G-T

87667125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111908205-G-C

http://identifiers.org/hco/13/GRCh38#87667204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111908286-A-C

87667236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111908317-G-T

87667237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111908318-T-C

87667259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111908339-A-G

87667274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111908354-T-G

87667285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111908365-C-T

87667345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111908426-T-C

http://identifiers.org/hco/13/GRCh38#87667592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111908678-C-A

87667592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111908678-C-T

http://identifiers.org/hco/13/GRCh38#87667671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111908718-C-A

87667671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111908718-C-T

87667853-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111908977-A-T

87667921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111909034-T-C

87667933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111909051-T-C

87668088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111909250-T-C

87668226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111909354-G-T

http://identifiers.org/hco/13/GRCh38#87668281-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111909410-A-C

87668621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111909680-G-A

87668664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111909731-A-G

87668829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111909899-T-C

http://identifiers.org/hco/13/GRCh38#87668961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111910038-A-C

87668962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111910039-T-C

87668970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111910047-A-G

87669162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111910193-A-T

87669233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111910269-T-C

87669426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111910453-C-T

87669460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111910489-C-G

87669586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111910600-A-T

87669599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111910610-G-A

87669644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111910641-T-C

http://identifiers.org/hco/13/GRCh38#87669724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111910717-A-C

http://identifiers.org/hco/13/GRCh38#87669815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111910803-C-A

87669815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111910803-C-T

http://identifiers.org/hco/13/GRCh38#87669925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111910906-A-C

http://identifiers.org/hco/13/GRCh38#87670044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111911021-C-A

87670475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111911437-T-C

87670520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111911492-C-T

87670551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111911520-T-G

87670617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111911583-T-A

87670617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111911583-T-C

87670824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111911781-A-G

87670843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111911800-A-G

87670862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111911815-G-T

87670892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111911842-A-G

87670892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111911842-A-T

87671022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 111911948-T-C

87671098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111912022-G-A

87671098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111912022-G-T

87671153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111912083-G-T

http://identifiers.org/hco/13/GRCh38#87671471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#111912397-C-A

http://identifiers.org/hco/13/GRCh38#87671674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#111912643-C-A

87672060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111913007-G-A

87672071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111913018-C-T

87672147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111913093-G-T

http://identifiers.org/hco/13/GRCh38#87672466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111913402-C-A

87672466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111913402-C-T

http://identifiers.org/hco/13/GRCh38#87672496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#111913432-C-A

87672496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111913432-C-T

http://identifiers.org/hco/13/GRCh38#87672744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#111913645-C-A

87672744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111913645-C-T

87672950-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111913803-T-A

87672950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111913803-T-C

87673099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111913951-C-T

87673271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111914179-C-T

87673363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111914271-G-A

87673469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111914388-G-A

87673489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111914408-G-A

87673489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111914408-G-T

87673627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111914531-G-A

87673686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111914594-T-C

87673732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111914643-G-T

87673888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111914796-G-A

87674083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111914930-G-T

87674135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42773
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111914970-G-A