7159007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10599683-G-A

http://identifiers.org/hco/10/GRCh38#7160106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10598583-C-A

7160287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10598425-T-C

7160342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10598365-T-C

7160371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10598335-A-G

7160459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10598248-T-C

http://identifiers.org/hco/10/GRCh38#7160512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10598195-C-A

7160512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10598195-C-T

7160529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10598178-T-C

http://identifiers.org/hco/10/GRCh38#7160537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10598170-C-A

7160539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10598168-A-T

7160792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10597977-A-G

7160868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10597917-G-A

7160868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10597917-G-T

7160920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10597862-T-C

http://identifiers.org/hco/10/GRCh38#7161017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10597761-C-A

7161017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10597761-C-T

7161075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10597708-G-T

http://identifiers.org/hco/10/GRCh38#7161315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10597470-C-A

7161418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10597373-G-A

7161418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10597373-G-T

http://identifiers.org/hco/10/GRCh38#7161460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10597330-C-A

7161460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10597330-C-T

7161495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10597315-T-C

7161526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10597284-G-A

7161557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10597267-G-T

7161637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10597175-T-C

7161686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10597125-A-G

7161710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10597100-G-T

http://identifiers.org/hco/10/GRCh38#7161711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10597099-A-C

http://identifiers.org/hco/10/GRCh38#7161915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10596904-C-A

7161915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10596904-C-T

7162005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10596784-G-A

7162005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10596784-G-T

7162074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10596712-G-A

7162074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10596712-G-T

7162076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10596710-T-C

http://identifiers.org/hco/10/GRCh38#7162084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10596702-C-A

7162084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10596702-C-T

7162098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10596688-T-G

7162139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10596654-G-A

7162234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10596581-G-A

7162235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10596580-C-T

7162293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10596538-T-C

7162402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10596445-G-T

7162455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10596395-T-A

7162465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10596385-C-T

7162477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10596373-T-G

7162565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10596264-G-A

7162638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10596147-C-T

http://identifiers.org/hco/10/GRCh38#7162641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10596144-C-A

http://identifiers.org/hco/10/GRCh38#7162730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10596056-C-A

7162730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10596056-C-T

7162769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10596021-A-G

7162778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10596010-C-G

7162778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10596010-C-T

7163256-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10595912-T-A

http://identifiers.org/hco/10/GRCh38#7163285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10595881-C-A

7163285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10595881-C-T

http://identifiers.org/hco/10/GRCh38#7163330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10595832-C-A

http://identifiers.org/hco/10/GRCh38#7163514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10595637-C-A

7163514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10595637-C-G

7163691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10595462-G-A

7163691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3 prime UTR variant
orthologous variants: 10595462-G-T

7163806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: synonymous variant
orthologous variants: 10595343-T-C

http://identifiers.org/hco/10/GRCh38#7163928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10595221-C-A

7163928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10595221-C-T

7163954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10595195-T-C

7164000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10595148-A-G

7164056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10595088-A-G

7164068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10595077-T-C

7164068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10595077-T-G

7164084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10595061-G-C

http://identifiers.org/hco/10/GRCh38#7164459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10594616-A-C

7164459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10594616-A-G

7164480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10594596-A-T

7164494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10594582-G-T

http://identifiers.org/hco/10/GRCh38#7164528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10594548-C-A

7164528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10594548-C-T

7164756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10594342-C-T

7164874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10593063-C-G

7164882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10593055-A-G

7164891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10593038-G-A

7165231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10592722-T-C

7165482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10592494-A-G

7165632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10592339-T-G

7165774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10592215-A-G

7165805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10592182-C-T

7165832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10592156-C-T

7166904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10589114-C-T

7167040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10588979-A-G

http://identifiers.org/hco/10/GRCh38#7167253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10588353-A-C

7167261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10588345-T-A

7167261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10588345-T-C

7167425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10588178-G-C

7167461-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10588130-A-T

7167485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10588105-G-A

7167524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10588066-C-T

7167573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10588022-C-T

7167710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10587910-T-C

7167721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10587900-C-G

7167808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10587802-A-G

7167867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10587765-C-T

7167897-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10587733-A-T

7168239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10587516-T-G

7168890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: intron variant
orthologous variants: 10586808-G-C

7171116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10585294-C-T

7171178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10585234-T-A

7171200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10585216-A-G

http://identifiers.org/hco/10/GRCh38#7171201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10585215-C-A

7171201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10585215-C-T

7171378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10584831-A-G

http://identifiers.org/hco/10/GRCh38#7171386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10584823-C-A

7171386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10584823-C-T

7171392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10584691-A-G

7171414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10584669-C-T

7171611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10584476-G-T

7171622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10584467-C-T

7171663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10584426-C-G

7171663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10584426-C-T

7171757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10584330-G-C

7171757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10584330-G-T

http://identifiers.org/hco/10/GRCh38#7171813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10584273-C-A

7171813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10584273-C-T

http://identifiers.org/hco/10/GRCh38#7171868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10584222-C-A

7171868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10584222-C-G

7171868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10584222-C-T

7171886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10584210-G-A

7171886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10584210-G-T

7171908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 10584188-G-A

7171908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 10584188-G-T

http://identifiers.org/hco/10/GRCh38#7171955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10584141-C-A

7171955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 10584141-C-T

7175001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10581521-A-T

7175110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10581417-G-A

7175144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10581385-C-T

7175244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10581289-A-G

7175457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10581078-C-T

7175482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10581052-T-G

7175595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10580900-G-A

7175633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10580849-C-T

7175777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10580544-C-T

7175855-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10580465-T-A

7175902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10580421-A-G

http://identifiers.org/hco/10/GRCh38#7176175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10580135-A-C

7176175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10580135-A-G

7176189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10580123-A-T

7176601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10578774-A-G

7176611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10578764-A-G

7176616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10578759-T-C

7176640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10578734-T-C

http://identifiers.org/hco/10/GRCh38#7176649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10578725-A-C

7176651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10578723-T-C

7176667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10578706-T-C

7176667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10578706-T-G

7176692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10578681-A-G

7176753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10578633-G-A

7176753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10578633-G-C

7179048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10577929-G-A

7179147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10577856-C-T

7179221-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10577795-A-T

7179258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10577758-C-T

7179600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10577459-C-T

http://identifiers.org/hco/10/GRCh38#7186815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10574446-C-A

7186815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10574446-C-G

7187167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10574108-T-G

7187207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10574068-G-A

7187426-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10573838-A-T

7188529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10573372-T-G

7188687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 10573216-A-G

7188768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10573138-A-G

http://identifiers.org/hco/10/GRCh38#7188776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10573130-C-A

http://identifiers.org/hco/10/GRCh38#7188852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10573073-A-C

7188852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10573073-A-G

7188852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10573073-A-T

7189001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10572934-T-G

7189063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10572909-A-T

7189104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10572873-T-C

7189232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10572535-T-A

7189235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10572532-A-G

7189333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10572431-T-A

7189333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10572431-T-C

7189333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10572431-T-G

7189444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10572375-C-T

7189530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10572320-T-C

7189600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10572257-C-T

7189601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10572256-G-A

7189670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10572187-T-C

7189728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10572114-C-T

7190068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10571910-G-A

7190068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10571910-G-T

7190178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10571813-G-A

7190364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10571630-C-T

7190426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10571567-G-A

http://identifiers.org/hco/10/GRCh38#7190739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10570891-A-C

7192307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10569428-A-T

http://identifiers.org/hco/10/GRCh38#7192991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10568001-C-A

7192991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10568001-C-T

7193230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10567783-G-A

7193426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10567604-G-A

7193541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10567508-G-C

7193541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10567508-G-T

7193546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10567503-G-A

7193834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10567310-C-T

7193857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10567295-G-A

7194157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10567160-C-T

7194168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10567149-C-T

7194370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10566929-C-T

http://identifiers.org/hco/10/GRCh38#7194427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10566873-A-C

http://identifiers.org/hco/10/GRCh38#7194517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10566776-A-C

7194517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10566776-A-G

7194651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10566640-G-A

7194713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10566575-C-T

http://identifiers.org/hco/10/GRCh38#7194999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10566292-C-A

7194999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10566292-C-G

7194999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10566292-C-T

7195010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10566281-C-T

7195169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10566112-A-G

7195234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10565833-C-T

7195249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10565818-G-C

7195444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10565624-T-C

7196199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10564024-G-A

7196199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10564024-G-T

7196215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10564009-C-T

7196724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10563496-G-A

7196982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10563256-G-A

7197018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10563207-G-A

7197035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10563192-C-T

7197075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10563155-A-G

7197185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10562849-T-C

7197242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10562790-C-T

7197249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10562785-C-T

7197264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10562770-G-A

http://identifiers.org/hco/10/GRCh38#7197373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10562679-A-C

7197405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10562647-G-A

7197405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10562647-G-T

http://identifiers.org/hco/10/GRCh38#7197488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10562563-C-A

7197488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10562563-C-G

7197488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10562563-C-T

7197511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10562544-G-A

7197511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10562544-G-C

7199523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10561933-A-G

7199672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10561806-C-T

7200008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10561593-C-T

7200142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10561356-C-T

7200174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10561324-T-C

7200281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10561227-T-C

7200282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10561226-G-A

7200282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10561226-G-T

http://identifiers.org/hco/10/GRCh38#7200392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10561123-C-A

7200392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10561123-C-G

7200392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10561123-C-T

http://identifiers.org/hco/10/GRCh38#7200393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10561122-C-A

7200393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10561122-C-T

7200403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10561112-G-A

http://identifiers.org/hco/10/GRCh38#7200425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10561087-A-C

7200425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 10561087-A-G

7200427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 10561085-G-A

http://identifiers.org/hco/10/GRCh38#7200506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10561007-C-A

7200506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10561007-C-G

7200506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10561007-C-T

7200534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560980-A-T

http://identifiers.org/hco/10/GRCh38#7200546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10560967-C-A

7200546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560967-C-T

7200596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560918-G-T

7200629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560885-T-C

7200716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560807-C-T

7200859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560704-C-T

7200877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560686-A-G

7200905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560658-G-A

7200905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560658-G-T

7200912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560651-G-A

7200912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560651-G-C

7200912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560651-G-T

7200925-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560638-T-A

7200925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560638-T-C

7200925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560638-T-G

7200934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560629-C-T

7200942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560621-A-G

7200968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560596-A-G

7200971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560593-G-A

7200971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560593-G-C

7200971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560593-G-T

7201019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560557-T-G

7201036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560540-G-T

7201064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560511-G-C

7201068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560507-C-T

7201076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560499-G-T

7201147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560425-C-T

7201312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560248-A-T

http://identifiers.org/hco/10/GRCh38#7201518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10560100-C-A

7201580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560034-C-T

7201610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10560005-C-T

7201774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10559846-A-G

7202140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10552552-A-T

7202235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10552494-G-A

7202235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10552494-G-T

7202236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10552493-T-A

7202236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10552493-T-C

7202236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10552493-T-G

http://identifiers.org/hco/10/GRCh38#7202263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10552466-C-A

7202263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10552466-C-T

7202267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10552462-G-A

7202267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10552462-G-T

7202288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10552448-T-A

7202288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10552448-T-C

7202292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10552444-G-A

7202292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10552444-G-T

7202294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10552442-A-T

http://identifiers.org/hco/10/GRCh38#7202326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10552410-A-C

7202326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10552410-A-G

7202339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10552397-G-T

http://identifiers.org/hco/10/GRCh38#7202360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10552390-C-A

7202360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10552390-C-G

7202360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10552390-C-T

7202574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10552193-G-A

7202575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10552192-T-C

7202645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10551783-T-G

7202674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10551755-A-G

7202755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10551676-C-T

7203001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10551484-G-A

7203002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10551483-C-T

7203578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10549926-G-T

7203587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10549917-G-C

7203587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10549917-G-T

7203608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10549896-G-A

7203608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10549896-G-T

7203640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10549864-A-G

7204369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10549562-C-T

7204434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10549129-T-C

7204434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10549129-T-G

7204502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10549074-A-G

7205610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10548052-T-C

7205665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10547996-A-T

7205671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10547990-G-T

7205673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10547989-T-C

7205673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10547989-T-G

7205691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10547971-T-C

7205691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10547971-T-G

7205694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10547970-G-A

7205755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10547923-C-T

7205826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 10547844-T-C

7205903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 10547767-G-T

7205953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10547717-G-A

7205990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10547694-G-A

7205991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10547693-A-G

7206044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10547639-A-G

7206143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10547555-G-C

http://identifiers.org/hco/10/GRCh38#7206196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10547518-C-A

7206196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10547518-C-T

7206242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10547476-C-T

7206547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10546862-C-G

7207585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10546445-G-T

7207802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10546236-G-C

7208750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10545629-T-C

7208750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10545629-T-G

7208782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10545597-A-G

7208842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10545538-A-T

7208848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10545532-G-A

7208945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10545437-G-T

7208997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10545380-A-T

7209003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10545374-G-A

7209003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10545374-G-C

7209855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10542795-C-G

7209887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10542769-T-C

7209974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10542686-T-C

http://identifiers.org/hco/10/GRCh38#7209987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10542673-A-C

7210146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10542511-G-A

7210146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10542511-G-C

7210309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10542359-T-C

http://identifiers.org/hco/10/GRCh38#7210316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10542352-A-C

7210316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10542352-A-G

7210412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10542264-G-C

7210579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10542097-T-C

7210579-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10542097-T-G

7210634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10542042-G-A

7210727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10541960-C-T

7210836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10541862-G-A

7210855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10541845-C-G

7210922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10541774-G-A

7210922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10541774-G-C

7210922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10541774-G-T

7217746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10538622-C-T

7217828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10538538-C-T

7217953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10538420-T-C

7218000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10538372-G-A

7218435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10537680-T-A

7218435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10537680-T-C

http://identifiers.org/hco/10/GRCh38#7218450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10537665-A-C

7218716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10537363-A-G

http://identifiers.org/hco/10/GRCh38#7219040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10537044-C-A

7219499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10536622-T-A

7219506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10536615-G-T

7219752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10536062-T-C

7219771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10536045-T-A

7219781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10536035-T-C

7220273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10535557-A-G

7220358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10535471-T-A

http://identifiers.org/hco/10/GRCh38#7220402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10535432-A-C

7220402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10535432-A-G

http://identifiers.org/hco/10/GRCh38#7220406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10535428-C-A

7220406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10535428-C-T

7220557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10535280-A-G

7222652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10537233-G-A

7223619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10532351-A-G

7223740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10532246-T-C

http://identifiers.org/hco/10/GRCh38#7224050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10532085-A-C

7224560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10531597-C-T

7224993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10531108-G-A

7225001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10531100-G-C

7225059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10531022-T-A

7225799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10530252-G-A

7225846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10530213-C-T

http://identifiers.org/hco/10/GRCh38#7227644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10529043-C-A

7227668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10529019-C-G

7227735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10528954-G-A

7227735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10528954-G-T

7227736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10528953-T-C

http://identifiers.org/hco/10/GRCh38#7227765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10528924-C-A

7227819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10528870-G-T

http://identifiers.org/hco/10/GRCh38#7227986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10528705-C-A

7227994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10528697-T-C

7228012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10528653-G-A

7228012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10528653-G-T

7228016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10528649-A-G

7228135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10528530-A-G

7231452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10527416-C-T

7231966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10526942-T-A

http://identifiers.org/hco/10/GRCh38#7231967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10526941-A-C

7232148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10526757-T-C

7232406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10526514-C-T

http://identifiers.org/hco/10/GRCh38#7232509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10526410-C-A

7232509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10526410-C-T

7232601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10526318-T-G

7232646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10526282-T-C

7234348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10523935-A-G

7234643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10523657-A-G

7234752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10523582-C-T

7238507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10469361-G-C

7238559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10469320-C-T

7238950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10468974-T-C

7239337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10468646-T-C

7239846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10468173-G-C

http://identifiers.org/hco/10/GRCh38#7242232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10467779-C-A

7242232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10467779-C-G

7242313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10467703-T-C

7242343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10467670-C-T

7242666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10467368-A-G

7242823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10467249-G-C

7242913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10467158-T-C

7243050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10466788-T-C

7243397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10466440-G-A

http://identifiers.org/hco/10/GRCh38#7243429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10466409-C-A

7243429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10466409-C-T

http://identifiers.org/hco/10/GRCh38#7243485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10466355-C-A

7243485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10466355-C-G

7243491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10466349-T-C

7243632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 10466207-C-G

7243684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 10466155-G-A

7243684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 10466155-G-T

7243810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10466028-T-A

7243819-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10466019-T-A

7243868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10465975-T-C

7243941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10465902-A-G

7244016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10465822-G-A

7244016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10465822-G-T

7244036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10465805-G-T

7244091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10465744-A-G

7244100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10465735-C-T

7244123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10465714-A-G

7244123-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10465714-A-T

7244126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10465711-C-T

7244138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10465699-G-T

7244190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10465646-C-G

7244210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10465626-G-A

7244210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10465626-G-T

7245408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10464161-C-T

7245565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10464018-G-A

7246216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10463400-A-G

7246262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10463355-A-G

7246292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10463332-G-T

http://identifiers.org/hco/10/GRCh38#7248046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -A-C

7248064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -T-A

7248079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -T-C

7248263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10462103-G-A

7248463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10461892-T-C

7248494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10461867-C-T

7248660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10461700-A-G

7248684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10461679-G-A

http://identifiers.org/hco/10/GRCh38#7248718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10461645-C-A

7248718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10461645-C-T

7248851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10461512-G-T

7249024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10461328-G-A

7249024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10461328-G-T

7249028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10461324-C-T

7249045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10461307-C-T

7249075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10461291-C-T

7249200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10461220-C-T

7249373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10461048-C-T

7249575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10460835-G-A

7249575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10460835-G-C

7249603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10460807-A-G

7252108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10460748-C-G

7252245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10460625-G-T

7252269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10460601-T-C

7258687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10459702-C-T

7258715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10459681-T-G

7258865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10459532-C-T

7258943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10459453-C-T

7259030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10459373-G-A

7263572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10456719-T-C

7263690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10456615-G-A

7263690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10456615-G-C

7264050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10455962-G-T

7264117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10455912-T-C

7264193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10455851-A-G

7264376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10455667-A-G

7264377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10455666-C-T

7270106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10453541-G-A

7270253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10453378-A-G

http://identifiers.org/hco/10/GRCh38#7270488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10453115-A-C

http://identifiers.org/hco/10/GRCh38#7270548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10453066-C-A

7270651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10452958-C-T

7270698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10452912-G-C

7270985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10452612-T-C

7276299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10451260-A-G

7276404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10451166-T-C

7276483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10451087-A-G

7276862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10450620-T-G

7276872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10450610-G-T

7276931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 10450552-A-G

7276986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 10450497-A-G

7277025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10450459-C-T

7277026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10450458-T-G

http://identifiers.org/hco/10/GRCh38#7277029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10450455-C-A

7277103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10450394-G-A

7277103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10450394-G-C

http://identifiers.org/hco/10/GRCh38#7277135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10450377-A-C

7277135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10450377-A-G

7277135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10450377-A-T

http://identifiers.org/hco/10/GRCh38#7277183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10450341-C-A

7277240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10450286-T-G

7277285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10450241-A-T

7277420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10450109-G-T

7277441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10450087-C-T

7277559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10449978-G-T

http://identifiers.org/hco/10/GRCh38#7277731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10449808-A-C

7277889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10449648-G-T

7278175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10449352-T-C

7279563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10449025-T-C

7279967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10448613-A-T

http://identifiers.org/hco/10/GRCh38#7279984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10448595-C-A

7280026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10448555-G-A

7280086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10448493-G-C

7280313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10448341-T-C

7280352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10448302-T-A

7280493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10448144-C-G

7280552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10448088-T-C

7281564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10447452-G-A

7281600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10447415-C-T

7281791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10447246-T-C

7282507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10446803-G-A

7282640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10446672-T-C

http://identifiers.org/hco/10/GRCh38#7282824-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10446345-A-C

7283068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10446102-T-C

7283201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10445960-G-C

7283456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10445632-G-A

7283633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10445201-A-G

7283657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10445177-G-A

http://identifiers.org/hco/10/GRCh38#7283783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10445040-A-C

7283814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10445009-G-T

7283874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10444954-C-T

7284048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 10444778-C-T

http://identifiers.org/hco/10/GRCh38#7284220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10444604-C-A

7284299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10444535-G-A

7284299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10444535-G-C

7284299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10444535-G-T

7284313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10444524-C-T

http://identifiers.org/hco/10/GRCh38#7284354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10444486-C-A

7284354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10444486-C-T

7284381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10444461-T-C

7284466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10444375-G-T

7284527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10444314-T-C

http://identifiers.org/hco/10/GRCh38#7284534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10444307-C-A

http://identifiers.org/hco/10/GRCh38#7284640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10444210-C-A

7284640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10444210-C-T

7284732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10443929-T-C

7284893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10443780-C-T

7284931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10443756-A-G

7284932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10443755-T-G

7285006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10443697-T-C

7285321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10443352-A-G

7285335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10443338-G-T

7285358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10443315-C-T

7285359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10443314-A-G

7285360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10443313-T-C

7285462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10443209-G-A

7285462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10443209-G-T

http://identifiers.org/hco/10/GRCh38#7285485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10443186-A-C

7285485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10443186-A-G

http://identifiers.org/hco/10/GRCh38#7285502-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10443164-A-C

7285502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10443164-A-G

http://identifiers.org/hco/10/GRCh38#7285507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10443159-C-A

7285507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10443159-C-G

7285507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10443159-C-T

7285586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10443115-G-T

7285596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10443105-A-T

7285605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10443096-A-G

7285662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10443043-G-A

7285662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10443043-G-T

7285673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10443032-G-A

7285673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10443032-G-T

http://identifiers.org/hco/10/GRCh38#7285832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, stop_lost
orthologous variants: http://identifiers.org/mco/2/GRCm39#10442878-A-C

7285942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 10442768-T-C

7285942-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 10442768-T-G

7286099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10442641-G-A

7286219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10442508-C-T

7286331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10442420-A-G

7286421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10442344-G-T

7286427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10442333-A-G

7289268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10440852-G-T

7289408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10440712-A-T

7289551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10440581-G-A

7289592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10440572-G-A

7289621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10440559-C-T

7289717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10440466-T-C

http://identifiers.org/hco/10/GRCh38#7298186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10440025-A-C

7298228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10439988-C-T

7298374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10439838-C-T

7298529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10439697-G-C

7298760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10439480-T-C

7303065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10438874-C-T

7303069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10438870-A-G

7303466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10438468-A-G

7311169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10436894-G-A

7311318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10436768-G-A

7311334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10436752-T-C

7311364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10436722-T-C

7311458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10436628-C-T

7311572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10436514-T-C

7312265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10436076-A-G

7312318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10436016-C-T

7312319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10436015-G-A

7312336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10435993-C-T

7312343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10435986-A-G

7312376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10435953-G-A

7312423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10435907-A-G

7312603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10435748-T-G

7312736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10435617-A-G

7312737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10435616-T-C

7312897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10435476-C-G

7314327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10434377-C-T

7314366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10434348-G-A

7316161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10432326-T-C

7316559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10432011-A-G

7316594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10431966-C-T

7316607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10431953-G-A

7316608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10431952-C-T

7316646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10431918-T-C

7316931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10431500-A-G

7317004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10431426-A-G

7317188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10431258-C-G

7317206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10431240-G-A

http://identifiers.org/hco/10/GRCh38#7317639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10429221-C-A

7317784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10429090-G-A

7317923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10429010-G-T

7318167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10428836-G-A

7318206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10428789-T-C

7318238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10428759-G-A

http://identifiers.org/hco/10/GRCh38#7320358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10427818-A-C

7320358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10427818-A-T

7320527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10427624-G-T

7331409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10426572-C-T

7331533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10426461-C-G

7341135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10425952-G-A

7341366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10425608-T-C

7341382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10425592-T-C

http://identifiers.org/hco/10/GRCh38#7341431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10425550-A-C

7341481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10425496-G-T

7341765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10425206-C-T

7342303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10424739-T-C

http://identifiers.org/hco/10/GRCh38#7342315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10424727-A-C

7344986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10423511-G-T

7344996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10423501-G-T

7345100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10423412-T-C

7345124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10423390-G-A

7345879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10422300-C-G

7345971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10422238-C-G

7345990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10422207-T-G

http://identifiers.org/hco/10/GRCh38#7346032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10422164-A-C

http://identifiers.org/hco/10/GRCh38#7346045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10422151-C-A

7347605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10420975-T-C

7347744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10420850-A-G

7347909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10420690-A-G

7347957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10420636-T-C

7347957-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10420636-T-G

http://identifiers.org/hco/10/GRCh38#7348054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10420548-C-A

7348091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10420517-A-G

7348108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10420500-T-A

7348204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10419820-G-A

7348204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10419820-G-T

7348206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10419818-G-A

7348206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10419818-G-C

7348206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10419818-G-T

7348224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10419803-G-A

7348224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10419803-G-C

7348224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10419803-G-T

7348261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10419765-T-C

7348274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10419752-G-A

7348274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10419752-G-C

7348274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10419752-G-T

7348275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10419751-A-G

7348275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10419751-A-T

7348300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 10419726-T-C

7348310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 10419716-C-T

http://identifiers.org/hco/10/GRCh38#7348367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10419655-C-A

7348367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10419655-C-T

7348376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10419649-G-A

7348376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10419649-G-T

http://identifiers.org/hco/10/GRCh38#7348388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10419636-C-A

7348388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10419636-C-T

7348403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10419619-G-A

http://identifiers.org/hco/10/GRCh38#7348409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10419613-C-A

7348409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10419613-C-T

7348767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10419265-G-A

7349960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10418502-G-T

http://identifiers.org/hco/10/GRCh38#7350071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10418409-C-A

7350109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10418369-G-C

7361191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10415697-T-C

7361631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10414977-T-C

7361655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10414952-G-A

7361655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10414952-G-T

7362032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10414566-G-A

7362727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10413786-A-G

7362800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10413695-A-G

7364020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10412440-A-T

7364304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10412158-G-C

7364309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10412153-T-A

7364339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10412123-G-C

7364613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10411851-T-C

7365994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10411421-G-C

7366031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10411343-G-A

7366058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10411308-T-C

http://identifiers.org/hco/10/GRCh38#7366307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10411097-A-C

7366423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10410981-T-A

7366423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10410981-T-C

7366544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10410835-C-T

7366626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10410756-C-T

7366627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10410755-G-A

http://identifiers.org/hco/10/GRCh38#7366641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10410741-C-A

7366941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10410496-G-C

7366977-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10410460-T-G

7367086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10410358-A-T

7367455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10409702-C-T

7367497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10409654-G-T

http://identifiers.org/hco/10/GRCh38#7367524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10409614-A-C

7367550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 10409588-T-C

http://identifiers.org/hco/10/GRCh38#7367600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10409536-C-A

http://identifiers.org/hco/10/GRCh38#7367736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10409400-C-A

7367798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 10409338-A-G

7367916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10409217-C-T

7367991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10409144-T-C

7367998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10409137-G-T

7368183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10408907-T-G

7368467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10408491-A-G

7368467-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10408491-A-T

http://identifiers.org/hco/10/GRCh38#7368485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10408465-C-A

7368642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10408196-C-G

7368848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10407995-T-C

7368866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10407977-T-A

7368919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10407932-T-C

7368952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10407903-G-C

7369507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10407622-G-T

7369579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10407555-T-C

http://identifiers.org/hco/10/GRCh38#7369611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10407524-C-A

7369611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10407524-C-T

7370174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10407001-T-C

http://identifiers.org/hco/10/GRCh38#7370175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10407000-C-A

7370175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10407000-C-T

http://identifiers.org/hco/10/GRCh38#7370179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10406996-C-A

7370179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10406996-C-G

7370179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10406996-C-T

7370195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10406978-T-A

7370195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10406978-T-C

7370195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10406978-T-G

http://identifiers.org/hco/10/GRCh38#7370246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10406927-C-A

7370246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10406927-C-T

http://identifiers.org/hco/10/GRCh38#7370253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10406920-C-A

7370468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10406748-G-T

http://identifiers.org/hco/10/GRCh38#7370482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10406734-C-A

7370482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10406734-C-T

7370483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10406733-C-T

7370523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10406693-C-T

7371769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10404344-G-A

7374844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10403592-G-C

http://identifiers.org/hco/10/GRCh38#7374852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10403584-C-A

http://identifiers.org/hco/10/GRCh38#7375328-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10403115-A-C

7375328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10403115-A-G

7376094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10402025-C-T

7376151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 10401970-T-C

7376404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10401740-T-C

7379710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10400424-C-T

7379754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10400380-T-C

7380014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10400172-T-C

7380129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10400080-T-C

7380200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10399522-A-G

http://identifiers.org/hco/10/GRCh38#7380317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10399401-A-C

http://identifiers.org/hco/10/GRCh38#7380377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10399341-C-A

7380648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10398926-G-A

http://identifiers.org/hco/10/GRCh38#7381671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10398326-C-A

7381906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 10398112-G-A

7381906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 10398112-G-T

http://identifiers.org/hco/10/GRCh38#7381918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10398099-C-A

7381918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 10398099-C-T

7381925-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 10398092-T-A

7381946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 10398073-T-A

7381946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 10398073-T-C

http://identifiers.org/hco/10/GRCh38#7381949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10398070-C-A

7381949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 10398070-C-T

7381964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10398055-A-G

7381998-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10398022-T-A

7381998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10398022-T-C

7381999-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10398021-T-A

7381999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10398021-T-C

7381999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10398021-T-G

http://identifiers.org/hco/10/GRCh38#7382005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10398015-C-A

7382005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10398015-C-G

7382005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10398015-C-T

http://identifiers.org/hco/10/GRCh38#7383452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10397155-C-A

http://identifiers.org/hco/10/GRCh38#7383453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10397154-C-A

7383698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10396935-C-T

7383706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10396927-G-C

7383706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10396927-G-T

7389820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10394749-T-C

7390035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10394535-C-T

7397796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10390037-G-A

7397977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10389839-T-C

7398237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10389566-G-A

7398322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10389481-C-G

7398942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10387093-C-T

7398943-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10387092-T-A

7403810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10385399-T-C

7404272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10385147-G-A

7404308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10385111-C-T

7404435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10385006-T-C

7404666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10384366-T-A

7405111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10383064-G-A

7405159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10383022-T-C

7405331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10382843-C-T

http://identifiers.org/hco/10/GRCh38#7405661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10382599-A-C

http://identifiers.org/hco/10/GRCh38#7405807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10382447-C-A

7405807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10382447-C-G

7405819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10382434-G-A

7405819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10382434-G-C

7405830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10382423-C-G

7405830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10382423-C-T

7405840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10382413-T-A

7405840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10382413-T-C

7405840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10382413-T-G

7405847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10382406-G-A

7405847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10382406-G-C

7405908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10382346-C-T

7405912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10382342-G-C

http://identifiers.org/hco/10/GRCh38#7406027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10382230-C-A

http://identifiers.org/hco/10/GRCh38#7406486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10381634-C-A

7406900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10381264-C-T

7406912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10381252-G-A

7406982-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10381197-T-G

7407233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10380946-T-A

7407233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10380946-T-C

7407233-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10380946-T-G

7407289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10380913-T-C

7407635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10380615-G-A

7407734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10380523-G-T

7407846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10380439-T-A

7407846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10380439-T-C

http://identifiers.org/hco/10/GRCh38#7408068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10380215-C-A

7408149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10380142-G-A

7408149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10380142-G-T

7408403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10379874-T-C

7408534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10379747-G-A

http://identifiers.org/hco/10/GRCh38#7408803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10379475-C-A

7409060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10379242-G-C

http://identifiers.org/hco/10/GRCh38#7409297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10379038-C-A

http://identifiers.org/hco/10/GRCh38#7409326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10379020-C-A

7409505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10378839-A-G

7409568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10378770-C-G

7409587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10378751-A-G

7409606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10378733-C-T

http://identifiers.org/hco/10/GRCh38#7409748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10378598-C-A

http://identifiers.org/hco/10/GRCh38#7409971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10378372-C-A

7409971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10378372-C-T

7409990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10378339-A-G

7410435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10377864-T-A

http://identifiers.org/hco/10/GRCh38#7410701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#10377592-C-A

7410729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10377565-T-C

7411410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5 prime UTR variant
orthologous variants: 10376874-A-G

7411466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5 prime UTR variant
orthologous variants: 10376817-G-A

7411466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20256
most severe consequence: 5 prime UTR variant
orthologous variants: 10376817-G-T