http://identifiers.org/hco/1/GRCh38#34712881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127295613-C-A

http://identifiers.org/hco/1/GRCh38#34712974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127295572-C-A

34712974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127295572-C-T

34713005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127295547-T-G

34713015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127295541-G-A

34713015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127295541-G-T

34713041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127295530-G-A

34713041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127295530-G-T

34713078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127295513-A-G

34713104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127295488-G-A

34713104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127295488-G-T

34713114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127295478-G-C

34713243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127295417-T-C

http://identifiers.org/hco/1/GRCh38#34713245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127295415-C-A

34713321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127295367-A-G

http://identifiers.org/hco/1/GRCh38#34713359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127295329-C-A

34713359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127295329-C-T

34713360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127295328-G-A

34713360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127295328-G-C

34713360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127295328-G-T

34713416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127295318-C-T

http://identifiers.org/hco/1/GRCh38#34713418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127295316-C-A

34713418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127295316-C-T

34713488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127295244-G-A

http://identifiers.org/hco/1/GRCh38#34713510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127295223-C-A

34713510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127295223-C-G

34713510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127295223-C-T

34713528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127295205-C-T

34713601-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127295149-A-T

34713644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127295111-G-T

34713669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127295086-T-C

34713670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127295085-A-G

34713680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127295074-G-A

http://identifiers.org/hco/1/GRCh38#34713754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127295000-C-A

34713757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127294997-G-A

34713779-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127294967-T-A

34713779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127294967-T-C

34713864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127294885-G-T

34713877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127294872-T-A

34713877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127294872-T-C

http://identifiers.org/hco/1/GRCh38#34713878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127294871-C-A

34713888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127294861-A-G

http://identifiers.org/hco/1/GRCh38#34713992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127294773-C-A

http://identifiers.org/hco/1/GRCh38#34714184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127294619-C-A

34714184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127294619-C-T

34714266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127294535-T-C

34714362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127294452-C-T

http://identifiers.org/hco/1/GRCh38#34714365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127294449-C-A

34714399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127294416-T-G

34714422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127294389-A-G

34714433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127294378-T-C

http://identifiers.org/hco/1/GRCh38#34714442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127294369-C-A

34714442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127294369-C-T

34714508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127294303-A-G

34714644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127294165-G-C

34714645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127294161-T-C

http://identifiers.org/hco/1/GRCh38#34714671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127294139-C-A

http://identifiers.org/hco/1/GRCh38#34714794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127294047-C-A

34714794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127294047-C-T

34714796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127294045-C-G

34714806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127294035-A-G

34714848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127294003-T-C

34714990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127293911-G-A

34715043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127293859-A-G

34715196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127293534-C-T

34715257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127293477-T-A

34715446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127293343-G-A

34715466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127293323-C-T

34715712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127293104-G-A

34715712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127293104-G-C

http://identifiers.org/hco/1/GRCh38#34715718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127293098-A-C

34715838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127292985-G-A

34715921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127292896-G-A

34716060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127291547-T-A

34716060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127291547-T-C

http://identifiers.org/hco/1/GRCh38#34716139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127291468-C-A

http://identifiers.org/hco/1/GRCh38#34716269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127291336-C-A

34716269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127291336-C-T

34716311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127291295-T-C

34716353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127291253-A-T

34716509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127291100-T-C

34716562-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127291047-T-A

34716565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127291044-T-C

34716565-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127291044-T-G

34716570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127291039-A-G

34716592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127291026-G-T

34716615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127291004-A-G

34719776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127290113-C-T

34719959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127289950-G-T

34719961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127289948-G-A

34720078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127289833-C-T

34720105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127289811-G-A

34720171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127289748-G-A

34720267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127289663-C-T

34720425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127289521-G-A

34720801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127289036-G-A

http://identifiers.org/hco/1/GRCh38#34720834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127289001-C-A

34720939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127288953-C-T

34721209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127288724-C-G

34721220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127288713-C-G

34721227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127288700-C-T

34721561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127288169-T-C

34721726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127287995-G-A

34721872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127287860-C-G

34725127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127282353-G-C

34725127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127282353-G-T

34725242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127282240-G-C

34725563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127281931-A-T

34725688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127281831-A-G

34725886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127281647-T-C

34725936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127281608-G-A

34725948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127281596-C-T

34726144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127281435-G-C

34726259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127281301-C-T

34726293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127281189-T-A

34726383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127281101-G-A

34726400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127281084-C-T

34726429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127281054-T-C

34726646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127280828-A-G

34726755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127280719-G-A

34726908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127280579-A-T

34726940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127280551-C-T

34726970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127280531-C-T

34727053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127280450-T-A

http://identifiers.org/hco/1/GRCh38#34727074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127280428-C-A

34727074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127280428-C-T

34727075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127280427-C-T

34727151-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127280351-T-A

34727164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127280335-G-A

34727164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127280335-G-T

34727220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127280270-T-G

34727307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127280111-C-T

http://identifiers.org/hco/1/GRCh38#34727441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127279898-A-C

34727463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127279800-G-A

34727575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127279696-A-T

34727577-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127279694-A-T

34727709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127279563-C-T

34727989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127279285-A-G

34728043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127279231-G-A

34728043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127279231-G-C

34728086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127279188-T-G

34729417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127278899-G-A

34729448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127278868-C-G

34729552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127278773-G-A

34729580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127278745-T-C

34729584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127278741-C-T

34729771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127278586-C-G

34729804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127278550-C-G

34730024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127278328-T-A

34730126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127278235-T-C

34730140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127278226-T-C

http://identifiers.org/hco/1/GRCh38#34730222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127278143-C-A

34730487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127277895-A-G

34730700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127277696-A-G

34730758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127277650-T-A

34730911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127277534-T-C

34730920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127277525-G-C

34730986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127277462-T-C

34730988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127277460-C-T

34731063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127277378-T-C

34731090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127277351-G-A

34731181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127277269-C-T

http://identifiers.org/hco/1/GRCh38#34731231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127277225-A-C

34731231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127277225-A-T

34731270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127277188-C-T

34731522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127276926-T-C

http://identifiers.org/hco/1/GRCh38#34731614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127276849-C-A

34731614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127276849-C-T

http://identifiers.org/hco/1/GRCh38#34731646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127276817-C-A

34731646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127276817-C-T

34731893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127276593-A-T

34732135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127276390-G-A

34732257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127276299-C-T

http://identifiers.org/hco/1/GRCh38#34732272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127276285-A-C

http://identifiers.org/hco/1/GRCh38#34732658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127275943-C-A

34733980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127275371-G-A

34734364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127274461-G-C

http://identifiers.org/hco/1/GRCh38#34735125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127271895-C-A

34735140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127271880-G-A

34736336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127270067-G-A

34736336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127270067-G-C

34736336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127270067-G-T

http://identifiers.org/hco/1/GRCh38#34736350-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127270056-A-C

34736539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127269904-T-C

34736602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127269819-T-C

34736812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127269647-G-A

34736840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127269619-G-T

34736892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127269570-A-T

34736893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127269569-G-A

34736902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127269560-C-T

34736928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127269534-G-A

34736967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127269514-C-T

34737140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127269339-T-C

34737327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127269192-G-A

34737433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127269085-C-G

34737433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127269085-C-T

34737504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127269057-C-G

34737504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127269057-C-T

34737508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127269053-G-A

http://identifiers.org/hco/1/GRCh38#34737579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127268999-C-A

34737910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127267651-C-T

34738058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127267523-C-G

34738325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127267325-C-T

34738522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127267128-A-G

34738566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127267073-G-A

34738579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127267060-G-T

34738589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127267048-C-T

34738654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127266987-C-T

34738772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127266862-G-C

34739663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127265712-T-C

34740451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127265096-A-G

34740673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127264044-G-A

http://identifiers.org/hco/1/GRCh38#34740732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127263939-C-A

34740783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127263887-A-G

http://identifiers.org/hco/1/GRCh38#34741119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127263544-A-C

34741160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127263502-C-T

34741178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127263484-C-T

34741205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127263457-G-T

34741532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127263170-T-C

34741739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127263084-C-T

34741882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127262948-G-A

34741905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127262933-G-A

34742225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127262656-G-A

34742354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127262573-C-T

34742803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127262382-G-A

http://identifiers.org/hco/1/GRCh38#34742819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127262366-C-A

34742821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127262364-C-T

34742890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127262297-G-A

34742949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127262258-C-G

34743027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127262187-G-A

34743104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127262108-T-G

34743178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127262055-T-A

34743178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127262055-T-C

34743217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127262019-T-C

34743415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127261887-G-C

34746059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127260521-C-T

34746065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127260515-G-A

34746271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127260375-C-T

34747340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127260030-G-A

34747352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127260018-G-A

http://identifiers.org/hco/1/GRCh38#34747353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127260017-C-A

34747353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127260017-C-T

34747946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127259486-T-C

34747975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127259460-T-A

http://identifiers.org/hco/1/GRCh38#34748838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127258704-C-A

34748994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127258584-G-A

34749124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127258476-T-G

34749249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127258376-C-G

http://identifiers.org/hco/1/GRCh38#34749273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127258345-A-C

http://identifiers.org/hco/1/GRCh38#34749477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127258190-C-A

34749477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127258190-C-G

http://identifiers.org/hco/1/GRCh38#34749539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127258127-C-A

34749564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127258102-G-A

34749564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127258102-G-T

34750074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127257595-T-G

34750310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127257376-G-T

34750538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127257173-C-T

34754992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127252034-G-T

34755006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127252020-G-C

34755006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127252020-G-T

http://identifiers.org/hco/1/GRCh38#34755014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127252012-A-C

34755014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127252012-A-T

34755082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127251925-T-G

34755147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127251872-T-C

http://identifiers.org/hco/1/GRCh38#34755153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127251865-C-A

34755153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127251865-C-T

34755170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127251842-G-A

34755170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127251842-G-T

34755461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127251582-T-G

34755544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127251502-G-A

34755644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127251431-T-C

http://identifiers.org/hco/1/GRCh38#34755777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127251310-A-C

34756505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127250748-A-G

34757158-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127250287-T-A

34757239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127250230-A-G

http://identifiers.org/hco/1/GRCh38#34757361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127250110-A-C

http://identifiers.org/hco/1/GRCh38#34757454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127250017-C-A

34757454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 127250017-C-G

34757454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 127250017-C-T

http://identifiers.org/hco/1/GRCh38#34757502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127249969-C-A

34757653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 127249818-C-T

34757736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 127249741-G-C

34758195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127249283-A-G

http://identifiers.org/hco/1/GRCh38#34758198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127249280-C-A

34758198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127249280-C-G

34758198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127249280-C-T

34758247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127249232-G-A

34758247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127249232-G-T

http://identifiers.org/hco/1/GRCh38#34758257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127249222-C-A

34758257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127249222-C-T

34758343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127249155-C-G

34758343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127249155-C-T

http://identifiers.org/hco/1/GRCh38#34758367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127249131-C-A

34758367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127249131-C-T

34758393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127249103-G-A

34758393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127249103-G-T

34758405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127249091-G-A

34758405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127249091-G-T

34758441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127249056-A-G

http://identifiers.org/hco/1/GRCh38#34758445-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127249052-A-C

34758445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127249052-A-G

34758527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127248973-G-T

34758635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127248916-G-A

34758635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127248916-G-T

34758638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127248913-G-A

34758811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127248758-T-C

34758990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127248592-A-G

34759368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127248237-A-G

34759850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127247780-T-C

34759888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127247742-G-A

34760304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127247344-G-T

34760563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127246601-G-A

34760595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127246568-G-A

34760785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127246382-G-C

34760785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127246382-G-T

34760963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127246238-A-T

http://identifiers.org/hco/1/GRCh38#34761055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127246139-C-A

34761083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127246114-T-C

34761083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127246114-T-G

34761189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127246004-G-A

34761189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127246004-G-C

34761207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127245990-G-A

34761390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 127245802-G-A

34761390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 127245802-G-C

34761450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 127245742-G-A

34761588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 127245604-A-G

34761693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 127245499-T-C

34761702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 127245490-C-T

34761807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 127245385-G-T

34761917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 127245275-C-T

34761999-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 127245193-A-T

http://identifiers.org/hco/1/GRCh38#34762102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127245095-C-A

34762102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127245095-C-T

http://identifiers.org/hco/1/GRCh38#34762106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127245091-C-A

34762106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127245091-C-G

34762106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127245091-C-T

http://identifiers.org/hco/1/GRCh38#34762238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127244960-C-A

34762238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127244960-C-G

34762238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127244960-C-T

34762340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127244865-G-T

34762370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127244854-G-A

34762370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127244854-G-T

34762374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127244850-G-A

34762374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127244850-G-T

34762385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127244835-T-A

34762385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127244835-T-C

http://identifiers.org/hco/1/GRCh38#34762455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127244777-C-A

34762455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127244777-C-G

34762455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127244777-C-T

34762478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127244760-T-A

34762478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127244760-T-C

34762478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127244760-T-G

34762680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127244579-G-A

34762743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127244513-T-C

34762813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127244473-T-A

34762813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127244473-T-C

34762826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127244454-G-A

34762826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127244454-G-T

http://identifiers.org/hco/1/GRCh38#34762970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127244313-C-A

34763015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127244269-A-G

http://identifiers.org/hco/1/GRCh38#34763020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127244264-A-C

34763023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127244261-T-C

http://identifiers.org/hco/1/GRCh38#34763100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127244184-C-A

34763100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127244184-C-T

34763211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127244056-T-A

34763211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127244056-T-C

34763257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127244006-G-T

http://identifiers.org/hco/1/GRCh38#34763347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127243917-C-A

34763347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127243917-C-T

http://identifiers.org/hco/1/GRCh38#34763355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127243902-C-A

34763355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127243902-C-G

http://identifiers.org/hco/1/GRCh38#34763566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127243734-C-A

34763604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127243692-T-C

34763727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127243573-A-T

34763743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127243552-A-G

34763765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127243530-G-A

34763765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127243530-G-T

34763855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127243453-A-G

34763872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127243436-A-G

34763872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127243436-A-T

34764543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127242840-G-A

http://identifiers.org/hco/1/GRCh38#34764582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127242802-C-A

http://identifiers.org/hco/1/GRCh38#34765210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127242187-C-A

34765393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127242018-A-G

34765830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127241590-T-C

34766062-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127241326-T-G

34766105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127241283-C-T

34766157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127241231-A-G

34766189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127241195-C-G

http://identifiers.org/hco/1/GRCh38#34766207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127241177-A-C

34767214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127240268-G-A

34767214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127240268-G-C

34767454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127240088-A-G

34767459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127240083-G-A

34769745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127236783-C-T

34770082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127236293-C-T

34770521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127235886-A-G

34770853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127235613-C-T

http://identifiers.org/hco/1/GRCh38#34770929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127235568-A-C

34770951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127235554-T-A

34770951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127235554-T-G

34771519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127235056-G-A

34776706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127229289-G-A

http://identifiers.org/hco/1/GRCh38#34776905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127229110-C-A

34776905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127229110-C-T

34777006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127229035-G-A

http://identifiers.org/hco/1/GRCh38#34777150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127228935-C-A

34777575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127228482-C-G

http://identifiers.org/hco/1/GRCh38#34777583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127228474-A-C

34777602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127228456-C-T

34777606-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127228452-A-T

34778111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127228127-G-A

34778158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127228098-G-A

34778158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127228098-G-C

34778214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127228047-T-C

34778371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127227942-C-T

http://identifiers.org/hco/1/GRCh38#34778419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127227889-A-C

34778419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127227889-A-G

34778468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127227831-G-A

34778490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127227814-G-A

34778518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127227786-T-C

34778787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127227587-C-G

34778787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127227587-C-T

34778811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127227562-C-T

34779528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127226177-T-C

34779607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127226101-T-C

34779657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127226057-G-A

34779772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127225922-G-A

34779772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127225922-G-C

34780135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127225550-G-A

34780288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127225409-T-G

http://identifiers.org/hco/1/GRCh38#34781226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127224860-C-A

34781302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127224786-G-A

http://identifiers.org/hco/1/GRCh38#34781304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127224783-C-A

34781304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127224783-C-T

34781533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127224560-T-C

34781736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127224335-G-A

34781736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127224335-G-C

34781736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127224335-G-T

34781825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127224261-G-A

34781825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127224261-G-T

34781832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127224254-G-A

34781832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127224254-G-T

http://identifiers.org/hco/1/GRCh38#34781844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127224236-A-C

34781844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127224236-A-G

34781851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127224229-G-T

34781928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127224147-G-A

34781928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127224147-G-T

34782005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127224030-C-G

34782099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127223898-G-C

34782118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127223880-T-C

34782129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127223869-G-A

34782129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127223869-G-C

34782129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127223869-G-T

http://identifiers.org/hco/1/GRCh38#34782207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127223766-C-A

34782275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127223699-G-T

34782330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127223667-T-G

34782714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127223347-G-T

34783174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127222959-G-A

34783203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127222926-G-A

34783209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127222918-C-G

34783556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127222538-G-T

http://identifiers.org/hco/1/GRCh38#34783687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127222420-A-C

34783687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127222420-A-G

34783727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127222382-G-A

http://identifiers.org/hco/1/GRCh38#34784749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127220551-C-A

34784749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127220551-C-T

34784868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 127220423-T-C

http://identifiers.org/hco/1/GRCh38#34785021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127220270-C-A

http://identifiers.org/hco/1/GRCh38#34785063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127220228-C-A

34785063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 127220228-C-G

34785063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 127220228-C-T

34785090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 127220201-G-A

34785090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 127220201-G-C

34785138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 127220153-G-A

http://identifiers.org/hco/1/GRCh38#34785567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127219724-C-A

http://identifiers.org/hco/1/GRCh38#34785611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127219701-A-C

http://identifiers.org/hco/1/GRCh38#34785627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127219685-C-A

34785627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127219685-C-T

http://identifiers.org/hco/1/GRCh38#34785658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127219654-C-A

34785664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127219648-G-T

http://identifiers.org/hco/1/GRCh38#34785761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127219551-C-A

34785761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127219551-C-T

34785779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127219540-T-C

34785889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127219435-G-A

34786012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127219325-C-T

34786094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127219267-A-G

34786131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127219235-G-C

34786131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127219235-G-T

34786133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127219233-G-T

34786146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127219209-C-G

34786146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127219209-C-T

34786149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127219206-A-G

http://identifiers.org/hco/1/GRCh38#34786174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127219196-C-A

34786201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127219175-C-G

http://identifiers.org/hco/1/GRCh38#34786272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127219143-C-A

34786298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127219117-G-T

34786452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127218950-A-G

34786483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127218918-G-A

34786483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127218918-G-C

34786483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127218918-G-T

34786498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127218905-G-T

http://identifiers.org/hco/1/GRCh38#34786512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127218891-C-A

34786512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127218891-C-T

34786515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127218888-G-A

34786515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127218888-G-T

34786556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127218853-G-A

34786582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127218836-G-C

http://identifiers.org/hco/1/GRCh38#34786606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127218809-A-C

34786620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127218795-T-C

34786989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127218518-G-A

34787115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127218401-C-G

34787115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127218401-C-T

34787188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127218328-C-T

34787322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127218212-G-A

34787322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127218212-G-T

34787853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127217640-G-A

34787853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127217640-G-T

34787890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127217603-A-T

34787910-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127217583-T-A

34787910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127217583-T-C

http://identifiers.org/hco/1/GRCh38#34787912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127217581-C-A

34787972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127217517-G-A

34787977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127217512-T-C

34792493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127208192-T-C

http://identifiers.org/hco/1/GRCh38#34792663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127208070-C-A

34792663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127208070-C-G

34793025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127207755-G-A

34793025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127207755-G-T

34793054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127207725-C-T

34793060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127207719-A-G

34793077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127207702-G-A

34793077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127207702-G-T

34793092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127207690-C-G

34793094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127207688-A-G

http://identifiers.org/hco/1/GRCh38#34793161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127207631-C-A

34793161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127207631-C-T

34793212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127207588-A-G

http://identifiers.org/hco/1/GRCh38#34793304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127207523-C-A

34793438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127207368-C-T

http://identifiers.org/hco/1/GRCh38#34793450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127207361-C-A

http://identifiers.org/hco/1/GRCh38#34793708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127207117-C-A

34793751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127207095-A-G

http://identifiers.org/hco/1/GRCh38#34794181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127206792-C-A

34794181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127206792-C-T

34794342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 127206631-A-G

34794349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 127206624-G-A

34794658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 127206315-G-A

34794658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127206315-G-T

34794679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 127206294-G-A

34794679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 127206294-G-T

34794760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 127206213-C-G

34794781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 127206192-G-A

34794874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 127206099-C-G

http://identifiers.org/hco/1/GRCh38#34794949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127206024-C-A

34795021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 127205952-G-A

34795210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 127205763-G-A

34795328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127205636-G-A

34795328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127205636-G-C

34795328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127205636-G-T

34795332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127205632-T-C

34795332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127205632-T-G

http://identifiers.org/hco/1/GRCh38#34795577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127205389-C-A

http://identifiers.org/hco/1/GRCh38#34795598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127205367-A-C

34795626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127205337-T-A

34795626-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127205337-T-G

34795668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127205291-A-T

34795774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127205183-T-C

34795804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127205132-T-C

34795804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127205132-T-G

34795805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127205131-G-A

34795805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127205131-G-C

34795805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127205131-G-T

34795828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127205109-G-T

34795832-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127205105-T-A

34795832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127205105-T-C

http://identifiers.org/hco/1/GRCh38#34796001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127204936-C-A

34796125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127204814-C-T

34797175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127203991-A-G

34797175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127203991-A-T

34797694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127203489-C-G

34797694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127203489-C-T

34797697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127203486-G-C

34797876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127203349-G-T

34797895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127203333-C-T

34797943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127203277-G-A

34798107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127203135-C-G

34798107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127203135-C-T

34798121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127203113-C-G

34798397-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127202509-T-A

34798623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127202282-A-G

34798746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127202159-T-A

34798891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127202021-T-C

34799042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127201919-A-T

34799082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127201879-T-C

34799993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127201365-C-G

http://identifiers.org/hco/1/GRCh38#34800038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127201313-A-C

34800038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127201313-A-T

34800077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127201278-A-G

34804293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127199844-C-T

34804294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127199843-A-G

34804455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127199703-C-T

34804677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127199505-C-T

34804685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127199497-G-C

34804870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127197879-C-G

34804969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127197782-T-C

34805056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127197686-C-T

34805891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127196482-T-C

http://identifiers.org/hco/1/GRCh38#34805902-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127196471-A-C

34805944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127196435-C-G

34806311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127196143-G-C

34806357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127196096-T-C

34806564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127195917-G-A

34824538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127184369-A-G

34824638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127184256-T-C

34824729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127184169-T-A

34825184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127183586-A-T

34826053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127182706-A-G

34827184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127182554-G-A

34827260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127182409-G-A

34827341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127182214-T-G

34827373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127182187-T-C

34827447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127182112-G-A

34827463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127182098-T-C

34827567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127182005-T-G

34827640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127181938-A-G

34827676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127181902-C-T

http://identifiers.org/hco/1/GRCh38#34828044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127181079-C-A

34828342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127180778-T-C

34828434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127180688-A-G

34828439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127180684-G-A

34828734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127180399-G-T

34829177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127178244-T-C

34829642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127177792-G-A

34829743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127177693-T-C

34829879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127177554-A-T

34830101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127174792-A-T

34830239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127174670-G-T

34830241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127174668-G-T

34830262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127174652-G-A

34831409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127174548-A-G

34831464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127174489-C-T

34831628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127174348-C-T

34831827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127174170-T-G

34832524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127173548-T-C

34832874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127173245-T-C

34832964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127173157-T-C

34832981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127173140-C-T

34833036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127173088-C-G

http://identifiers.org/hco/1/GRCh38#34833042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127173082-C-A

34835730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127172662-C-T

34835898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127172500-C-T

34836007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127172400-A-G

34836037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127172375-G-C

34836243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127172185-G-T

34836452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127171984-T-G

http://identifiers.org/hco/1/GRCh38#34836521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127171917-A-C

http://identifiers.org/hco/1/GRCh38#34836538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127171899-A-C

34836568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127171874-C-T

34838309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127169704-A-G

34838513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127169507-T-C

34841163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127169192-T-A

34841166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127169189-T-C

34841208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127169155-G-A

http://identifiers.org/hco/1/GRCh38#34841367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127169002-C-A

34841450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127168946-C-T

34841527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127168870-A-G

34841798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127168590-C-G

34841824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127168561-G-A

34841824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127168561-G-C

34842177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127158631-T-C

34842228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127158581-G-A

34842235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127158562-T-C

34842329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127158481-C-T

34842331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127158479-C-G

34842331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127158479-C-T

34842412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127158398-A-G

34842486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127158332-T-A

34842768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127158221-A-G

34842776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127158213-C-G

34842800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127158190-T-C

34842802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127158188-T-C

34842865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127158107-T-C

http://identifiers.org/hco/1/GRCh38#34843099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127157875-C-A

34843100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127157874-C-G

34843153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127157821-G-T

http://identifiers.org/hco/1/GRCh38#34843293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127157677-C-A

34843542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127157435-C-T

34843916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127157081-G-A

34844080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127156942-T-C

34844097-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127156925-T-G

34844299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127156759-G-A

34844344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127156723-C-G

34844344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127156723-C-T

34844390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127156676-C-T

34845436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127155937-A-G

34845599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127155779-G-A

34845599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127155779-G-C

34847168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127152430-C-T

34847350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127152253-G-A

34847350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127152253-G-C

34847355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127152248-G-T

34847851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127150833-G-A

34848096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127150579-G-A

34848543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127150192-C-T

34848634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127150111-T-C

34850036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127147796-C-T

34850078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127147753-G-C

34850159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127147659-G-A

34850159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127147659-G-C

34850159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127147659-G-T

34850690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127147181-A-G

34850730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127147133-G-A

34850730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127147133-G-T

34850932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127146985-T-C

34851328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127146545-G-A

34851334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127146539-G-C

http://identifiers.org/hco/1/GRCh38#34851608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127146048-C-A

34851608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127146048-C-T

34851642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127146014-G-A

34851811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127145848-A-G

34852068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127145580-T-A

34852408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127145239-G-A

34852730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127144113-G-A

http://identifiers.org/hco/1/GRCh38#34852734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127144109-C-A

34852789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127144052-T-A

34852789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127144052-T-C

34852789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127144052-T-G

34852812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127144016-G-A

34852812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127144016-G-T

34852912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127143907-C-T

34852921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127143898-G-A

34852921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127143898-G-T

http://identifiers.org/hco/1/GRCh38#34852998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#127143780-C-A

34852998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127143780-C-G

34852998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127143780-C-T

34853087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 127143696-A-G

34853263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127143558-T-C

34853268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127143553-G-A

34853419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127143457-A-G

34853714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127142675-G-A

34853714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127142675-G-C

34853714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127142675-G-T

34853841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127142562-G-A

34853841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127142562-G-T

34853873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127142531-C-G

34853873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127142531-C-T

34853891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127142513-G-A

34853891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127142513-G-T

34853932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127142480-A-G

http://identifiers.org/hco/1/GRCh38#34853962-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127142453-A-C

34853962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127142453-A-G

http://identifiers.org/hco/1/GRCh38#34854011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127142411-A-C

34854077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127142324-A-G

34854105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127142307-G-A

34854105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127142307-G-C

34854105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127142307-G-T

34854424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127142076-T-C

34854448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127142052-T-C

34854450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127142050-T-A

http://identifiers.org/hco/1/GRCh38#34854535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127141996-C-A

34854535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127141996-C-T

34854548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127141983-G-A

34854548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127141983-G-T

34854724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127141875-G-T

http://identifiers.org/hco/1/GRCh38#34854854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127141773-C-A

34854854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127141773-C-T

34854890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127141737-G-A

34854890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127141737-G-T

34854898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127141729-A-G

http://identifiers.org/hco/1/GRCh38#34854968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127141666-C-A

34854968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127141666-C-T

34854981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127141657-G-T

http://identifiers.org/hco/1/GRCh38#34854999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127141644-C-A

34854999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127141644-C-T

34855026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127141619-G-C

34855026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127141619-G-T

34855054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127141593-C-T

http://identifiers.org/hco/1/GRCh38#34855083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127141567-A-C

34855083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127141567-A-G

34855094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127141555-G-A

http://identifiers.org/hco/1/GRCh38#34855104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127141545-A-C

34855104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127141545-A-G

34855104-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127141545-A-T

http://identifiers.org/hco/1/GRCh38#34855122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127141527-C-A

http://identifiers.org/hco/1/GRCh38#34855322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127141347-C-A

34855322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127141347-C-G

http://identifiers.org/hco/1/GRCh38#34855395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127141276-C-A

34855395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127141276-C-T

34855472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127141195-G-A

34855493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127141174-G-T

34855545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127141127-C-G

34855545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127141127-C-T

34855629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127141044-G-C

34855799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 127140877-T-C

34856024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127140649-T-A

34856024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127140649-T-C

http://identifiers.org/hco/1/GRCh38#34856048-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127140625-A-C

34856048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127140625-A-T

34856069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127140606-G-A

34856069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127140606-G-T

34856448-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127140497-T-A

34856483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 127140466-A-G

34856678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127140298-C-T

http://identifiers.org/hco/1/GRCh38#34857214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127139986-C-A

34857469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 127139714-G-T

34857482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127139701-C-T

34857540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127139657-G-T

http://identifiers.org/hco/1/GRCh38#34857557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127139645-C-A

34857557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127139645-C-T

34857734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127139452-C-G

34857734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127139452-C-T

34858191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127139356-A-T

http://identifiers.org/hco/1/GRCh38#34858213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127139334-C-A

34858271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127139278-G-A

http://identifiers.org/hco/1/GRCh38#34858385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127139182-C-A

http://identifiers.org/hco/1/GRCh38#34858417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127139148-C-A

34858417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127139148-C-T

34858430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127139135-G-A

34858439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127139126-A-T

http://identifiers.org/hco/1/GRCh38#34858486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127139082-C-A

34858520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127139048-T-C

34858531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127139037-A-G

http://identifiers.org/hco/1/GRCh38#34858765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127138497-C-A

http://identifiers.org/hco/1/GRCh38#34858936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127138332-C-A

34858936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127138332-C-T

http://identifiers.org/hco/1/GRCh38#34859011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127138247-C-A

34859171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127138111-C-T

34859179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127138103-G-A

34859185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127138096-C-T

34859315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127137995-G-T

http://identifiers.org/hco/1/GRCh38#34859406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127137917-C-A

34859492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127137850-G-A

34859492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127137850-G-T

34859493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127137849-T-C

http://identifiers.org/hco/1/GRCh38#34859572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#127137813-C-A

34859572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127137813-C-T

34859573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127137812-A-G

34859616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127137770-C-T

34859632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 127137741-C-T

34859746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25154
most severe consequence: 5 prime UTR variant
orthologous variants: 127137618-C-T