168695490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: 164651810-T-A

168695553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: 164651760-G-A

168695553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: 164651760-G-T

http://identifiers.org/hco/1/GRCh38#168695569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164651743-A-C

168695569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: 164651743-A-G

168695572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: 164651740-T-C

168695654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: 164651687-G-T

http://identifiers.org/hco/1/GRCh38#168695662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164651685-C-A

168695662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: 164651685-C-T

168695670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: 164651677-G-T

http://identifiers.org/hco/1/GRCh38#168695739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164651608-C-A

168695933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: 164651437-C-G

http://identifiers.org/hco/1/GRCh38#168695934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164651436-C-A

168695934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: 164651436-C-T

168695965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: 164651402-T-C

168695971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: 164651396-T-C

168696045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: 164651322-C-T

168696075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: 164651293-C-G

168696075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: 164651293-C-T

168696080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: 164651288-A-G

http://identifiers.org/hco/1/GRCh38#168696095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164651264-C-A

168696095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: 164651264-C-G

168696235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: 164651118-G-A

168696314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: 164651037-A-G

http://identifiers.org/hco/1/GRCh38#168696318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164651033-C-A

http://identifiers.org/hco/1/GRCh38#168696350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164651001-C-A

168696352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: 164650999-T-C

168696352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: 164650999-T-G

168696431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: 164650920-G-C

168696431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: 164650920-G-T

168696482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: 164650876-T-G

168696537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 3 prime UTR variant
orthologous variants: 164650815-T-A

168696571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: missense variant
orthologous variants: 164650781-T-A

168696670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164650691-G-A

168696671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164650690-A-G

168696678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164650683-G-T

168696679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164650682-C-T

http://identifiers.org/hco/1/GRCh38#168696723-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164650640-A-C

168696723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164650640-A-G

168696844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164650538-G-A

168696895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164650499-A-G

168697341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164650387-G-A

168697678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164650065-A-G

168697686-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164650057-T-G

168697727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164649999-G-A

168697882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164649841-C-T

http://identifiers.org/hco/1/GRCh38#168697957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164649766-A-C

168697978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164649749-T-C

168698085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164649662-C-G

168698141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164649599-T-G

168698144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164649596-T-C

168698164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164649573-C-T

168698251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164649482-T-C

168698291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164649453-T-C

168698294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164649450-G-C

168698596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164649151-G-T

http://identifiers.org/hco/1/GRCh38#168698738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164649000-A-C

168698761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164648991-A-G

168698791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164648958-G-A

168698804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164648944-A-T

168699248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164648500-G-A

168699291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164648451-T-A

168699331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164648422-C-T

http://identifiers.org/hco/1/GRCh38#168699570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164648206-C-A

http://identifiers.org/hco/1/GRCh38#168699617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164648180-C-A

168699617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164648180-C-T

168699845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164647949-T-C

168699993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164647765-C-T

168700160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164647539-C-T

168700372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164647124-A-T

168700469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164647023-C-G

168700561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164646928-C-T

168700616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164646885-C-T

168700628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164646873-G-A

168700681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164646813-C-T

168700767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164646727-C-T

168700950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164646638-A-G

168700951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164646637-T-C

168701056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: missense variant
orthologous variants: 164646530-T-C

http://identifiers.org/hco/1/GRCh38#168701127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164646459-A-C

168701127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 164646459-A-G

168701127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 164646459-A-T

http://identifiers.org/hco/1/GRCh38#168701196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164646420-C-A

168701196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164646420-C-T

168701198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164646418-A-G

168701208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164646408-G-T

http://identifiers.org/hco/1/GRCh38#168701229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164646394-C-A

http://identifiers.org/hco/1/GRCh38#168701358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164646286-C-A

168701419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164646218-T-C

168701461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164646176-A-G

168701473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164646167-A-G

168701479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164646161-C-G

168701479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164646161-C-T

168701501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164646139-T-C

168703479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164645727-C-G

168703479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164645727-C-T

168703482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164645724-T-C

http://identifiers.org/hco/1/GRCh38#168703600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164645612-C-A

168703600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164645612-C-G

168703691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164645531-G-A

168703791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164645459-C-T

168703891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164645364-G-A

168703918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164645341-T-C

168703954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164645309-G-A

168703961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164645302-A-G

168704071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164645192-C-T

168704110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164645157-C-T

168704268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164645013-C-G

168704289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164644992-T-C

168704292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164644989-A-G

168704331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164644961-G-A

http://identifiers.org/hco/1/GRCh38#168704378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164644908-C-A

168706142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164644555-G-A

168706177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164644520-C-G

168706272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164644425-T-C

168706875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164642955-C-G

168706875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164642955-C-T

168706914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164642927-C-T

http://identifiers.org/hco/1/GRCh38#168706957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164642882-C-A

168706957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164642882-C-T

168707029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164642803-C-T

168707101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164642725-G-A

http://identifiers.org/hco/1/GRCh38#168707215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164642663-C-A

http://identifiers.org/hco/1/GRCh38#168707223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164642655-C-A

168707223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164642655-C-T

168707284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164642602-C-T

168707298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164642588-T-C

168707315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164642571-C-G

168707315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164642571-C-T

168707389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164642514-G-T

168707538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164642386-G-T

168707540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164642384-G-A

168708339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164642302-G-A

168708438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164642210-A-G

168708754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164642035-C-T

168708828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron_variant, undefined
orthologous variants: 164641965-G-A

http://identifiers.org/hco/1/GRCh38#168708961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#164641817-A-C

168708961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron_variant, undefined
orthologous variants: 164641817-A-G

http://identifiers.org/hco/1/GRCh38#168709025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#164641749-C-A

168709092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron_variant, undefined
orthologous variants: 164641677-T-A

168709092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron_variant, undefined
orthologous variants: 164641677-T-C

168709115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron_variant, undefined
orthologous variants: 164641661-A-G

168709296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron_variant, undefined
orthologous variants: 164641455-T-C

168709342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron_variant, undefined
orthologous variants: 164641405-G-A

http://identifiers.org/hco/1/GRCh38#168709600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164641152-C-A

168709697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164641063-G-C

168709811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164640570-G-T

168709997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron_variant, undefined
orthologous variants: 164640112-T-C

168710052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164640066-G-A

http://identifiers.org/hco/1/GRCh38#168710070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#164640052-A-C

168710408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164639739-G-A

http://identifiers.org/hco/1/GRCh38#168710455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164639694-A-C

168710455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164639694-A-G

168710496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164639659-T-C

168710600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164639548-G-T

168710609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164639538-T-G

168710658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164639489-C-T

168710857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164639328-G-A

168710857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164639328-G-T

http://identifiers.org/hco/1/GRCh38#168711271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164639205-C-A

168711271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164639205-C-T

168711384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164639143-G-A

168711637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164638906-T-C

168711959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164638594-G-A

168711959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164638594-G-C

168713043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164637657-G-C

http://identifiers.org/hco/1/GRCh38#168713049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164637651-C-A

168713080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164637621-C-T

168713126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164637577-G-T

168713186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164637517-C-T

168713191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164637512-G-C

168713218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164637498-G-A

168713222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164637494-T-C

168713252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164637464-C-G

168713338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164637394-T-G

168713471-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164637265-T-A

168713654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164637088-G-A

http://identifiers.org/hco/1/GRCh38#168713715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164637028-C-A

168713715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164637028-C-T

168713716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164637027-A-G

168713803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164636946-G-T

168713869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164636892-G-A

http://identifiers.org/hco/1/GRCh38#168714109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164636717-C-A

168714109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164636717-C-G

168714109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164636717-C-T

168714126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164636700-G-T

168714153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164636672-C-T

168714168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164636657-G-A

168714312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: missense variant
orthologous variants: 164636507-C-T

168714395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164636435-G-A

http://identifiers.org/hco/1/GRCh38#168714397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164636433-C-A

168714397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164636433-C-T

168714448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164636385-A-T

168714534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164636306-T-C

168714926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164636029-A-G

168715913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164635283-T-C

168715965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164635235-G-C

168716251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164634111-C-T

168718244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164633506-T-C

168718246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164633504-G-T

168718289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164633461-C-T

168718292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164633458-T-C

168718390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164633361-A-G

168718509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164633246-T-G

168718776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164632985-A-G

168718922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164632842-G-A

168718922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164632842-G-C

168718954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164632810-A-G

168719000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164632769-G-C

168719112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164632620-A-G

168719112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164632620-A-T

168719295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron_variant, undefined
orthologous variants: 164632427-C-T

168719318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164632400-C-T

168719321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164632397-T-C

168719337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164632381-T-C

168719506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164632200-C-G

168719506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164632200-C-T

168719564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron_variant, undefined
orthologous variants: 164632142-A-G

168719877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164631943-T-C

168720111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164631712-G-A

168720132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164631691-T-C

168720585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164631145-G-A

168720585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164631145-G-C

168720746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164630976-C-G

168720987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164630773-A-G

168721137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164630674-T-C

168721142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164630665-G-A

168721142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164630665-G-C

168721142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164630665-G-T

http://identifiers.org/hco/1/GRCh38#168721225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164630574-C-A

http://identifiers.org/hco/1/GRCh38#168721560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164630472-A-C

168721594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164630457-G-A

168721643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164630409-T-G

168721664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164630397-A-G

168721731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164630335-G-A

168721750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164630310-A-G

168721767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164630287-A-T

168721855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164630206-C-G

168721894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164630174-C-T

168721988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164630099-C-T

168722092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164630046-C-T

168722141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164630000-A-G

http://identifiers.org/hco/1/GRCh38#168722295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164629856-A-C

168722295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164629856-A-G

http://identifiers.org/hco/1/GRCh38#168722986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164629046-A-C

168723155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164628889-G-A

168723161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164628883-T-A

168723866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164628268-A-G

168723910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164628238-A-G

168723920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164628228-C-T

168724306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164627839-G-T

168724959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164627711-A-G

168724959-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164627711-A-T

168724961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164627709-A-G

168725604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164627244-C-T

168725647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164627206-T-C

168725802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164627081-T-C

168726098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164626780-T-C

168726125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164626753-G-A

168726284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164626657-T-C

168726284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164626657-T-G

168726410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164626534-A-G

168726439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164626505-A-G

168726486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164626467-C-G

168726703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164626241-A-G

168727105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164625873-G-C

168727316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164625698-A-G

168727350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164625668-A-G

http://identifiers.org/hco/1/GRCh38#168727981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164625437-A-C

168728013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164625407-T-C

168728026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164625394-G-C

168728070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164625350-C-G

168728070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164625350-C-T

168728107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164625324-A-G

168728198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164625240-A-G

168728309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164625113-A-G

168728384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164625035-G-A

168728389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164625030-G-A

168728396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164625023-C-T

168728432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164624993-G-A

168728576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164624870-G-A

http://identifiers.org/hco/1/GRCh38#168728586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164624860-A-C

168728594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164624851-C-T

168728698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164624756-G-A

168728723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164624732-T-C

168728777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164624686-T-A

168728778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164624685-T-A

168728778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164624685-T-C

168728822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: intron variant
orthologous variants: 164624646-A-G

168729163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: synonymous variant
orthologous variants: 164624310-A-G

http://identifiers.org/hco/1/GRCh38#168729179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164624294-C-A

168729179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3011
most severe consequence: 5 prime UTR variant
orthologous variants: 164624294-C-T