http://identifiers.org/hco/6/GRCh38#17393625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#46655577-C-A

17393625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 46655577-C-G

17393625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 46655577-C-T

17393703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 5 prime UTR variant
orthologous variants: 46655646-C-T

17393732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 46655675-A-G

17393793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46655732-G-A

17393793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46655732-G-T

17393796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46655735-C-T

17393797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46655736-A-G

17393863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46655815-C-T

17393895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46655849-G-A

17393896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46655850-G-A

17393896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46655850-G-T

http://identifiers.org/hco/6/GRCh38#17394020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46655964-C-A

17394038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46655982-G-C

http://identifiers.org/hco/6/GRCh38#17394091-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46656032-A-C

17394108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46656048-C-T

17394188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46656128-C-T

17394631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46656628-A-G

http://identifiers.org/hco/6/GRCh38#17394649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46656657-A-C

17394649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46656657-A-G

17394655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46656681-G-A

17394704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46656915-G-A

17394808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46657018-A-G

17394809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46657019-A-G

17394916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46657106-G-A

17394956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46657142-A-T

17395003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46657201-T-C

17395011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46657209-G-A

17395011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46657209-G-T

17395092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46657281-C-T

17395138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46657319-G-A

17395218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46657391-G-A

17395231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46657404-G-C

17395577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46657856-G-A

17396200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46658755-G-A

17396282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46658815-C-T

http://identifiers.org/hco/6/GRCh38#17397975-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46661575-A-C

17397975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46661575-A-G

17399377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46661795-T-C

17399416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46661828-G-A

17399424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46661836-T-C

17399521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46661988-A-G

17400492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46662435-A-G

17412498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46667952-A-G

17412560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46668024-T-C

17412621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46668082-A-G

17412674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46668132-T-C

17413095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46668410-G-A

17413171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46668488-G-T

17413183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46668500-G-T

17413194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46668511-A-G

http://identifiers.org/hco/6/GRCh38#17413425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46669059-A-C

17413456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46669083-T-A

17413591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46669202-A-G

17413591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46669202-A-T

17413700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46669282-C-G

http://identifiers.org/hco/6/GRCh38#17414159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46669412-A-C

17414243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46669447-T-C

17415154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46670371-C-T

17415209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46670426-A-G

17415401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46670645-T-C

17415530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46670766-T-C

17415884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46671112-G-A

17417157-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46675505-T-A

17417737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46676155-G-C

17417810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46676225-C-T

17417947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46676391-T-C

17418004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46676440-T-C

17418180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46676580-A-G

17418490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46676847-G-A

17418506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46676867-G-A

17418518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46676879-G-A

17418764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46677111-T-C

17418803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46677150-C-T

17419230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46677566-A-G

http://identifiers.org/hco/6/GRCh38#17419269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46677603-A-C

17419340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46677672-T-C

17419342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46677674-T-C

17419457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46677789-A-G

17419614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46677885-C-T

17420762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46678494-G-A

17420776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46678508-G-T

17421447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46678787-T-A

http://identifiers.org/hco/6/GRCh38#17421451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46678791-C-A

17421451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46678791-C-T

17421559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 46678895-G-A

17421566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 46678902-T-C

17421688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46679024-A-G

17421704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46679040-G-A

17421726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46679062-T-C

17421781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46679114-T-C

17421791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46679124-A-G

17421845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46679178-G-C

17421855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46679188-C-G

17421855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46679188-C-T

17422018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46679244-G-A

17422105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46679331-C-G

17422124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46679349-A-G

17423121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46681051-T-C

17423145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46681074-A-G

17423208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46681138-C-T

17423384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46681264-C-G

17423385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46681265-T-C

17423495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46681360-A-G

17423600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46681459-G-A

http://identifiers.org/hco/6/GRCh38#17423636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46681488-C-A

17423856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46682002-C-T

17423964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46682119-T-G

17423972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46682120-T-A

17424128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46682168-G-A

17424170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46682210-G-T

17424495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46682497-T-C

17424642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46682647-A-T

17424730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46682734-G-A

17424746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46682759-C-T

17424829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46682845-G-A

http://identifiers.org/hco/6/GRCh38#17425308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46683357-A-C

http://identifiers.org/hco/6/GRCh38#17425400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46683459-A-C

17425400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46683459-A-G

17426525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46684387-G-A

17426592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 46684455-G-A

17426612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 46684475-C-T

17426761-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46684587-A-T

17426912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46684684-T-A

17426935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46684716-A-T

17427041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46684829-G-A

17427178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46684989-A-G

17427240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46685058-A-G

17427260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46685082-A-G

17427654-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46685447-T-A

17427659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46685452-G-A

17427727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46685516-T-C

17427886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46685607-C-T

17427971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46685693-G-A

17428011-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46685734-T-A

17428069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46685789-A-G

17429127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46686937-T-A

17429417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46687188-G-A

17429442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46687213-T-C

17429819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46687666-G-A

17429935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46687781-G-A

17430346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46688230-A-G

17430474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46688337-G-A

17430487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46688353-C-T

http://identifiers.org/hco/6/GRCh38#17430533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46688401-A-C

17430533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46688401-A-T

17430919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46688705-G-A

17431023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46688783-A-G

17431023-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46688783-A-T

http://identifiers.org/hco/6/GRCh38#17431434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46688908-A-C

17432430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46689303-T-C

17432439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46689312-A-T

17433470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46690129-C-T

17433571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46690238-G-A

17433958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46690931-G-C

17433958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46690931-G-T

17441052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46693605-A-G

17441375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46694010-T-C

http://identifiers.org/hco/6/GRCh38#17441445-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46694077-A-C

17441484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46694112-A-G

17441934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46694440-T-A

17441936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46694442-A-T

17442249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46694753-C-T

http://identifiers.org/hco/6/GRCh38#17442271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46694775-A-C

17442281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46694785-T-C

http://identifiers.org/hco/6/GRCh38#17442317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46694844-C-A

17442366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46694896-G-A

17442407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46694936-C-T

17442418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46694947-A-G

17442464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46694992-T-C

17442488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46695082-G-A

17443634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46696647-C-T

17443712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46696721-G-A

17443826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46696829-T-C

17444245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46697341-A-G

17444283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46697379-G-A

http://identifiers.org/hco/6/GRCh38#17444749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46697526-A-C

17444912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46697680-G-A

17445820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46698252-T-C

17446282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46698678-T-A

17446342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46698764-T-C

17446373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46698796-A-T

17446417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46698836-G-A

17446576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46698983-A-G

17446665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46699072-A-G

17448062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46700287-T-C

17449278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46701607-A-G

17449884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46701834-T-C

17449917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46701867-T-C

17449974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46701924-C-T

17450012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46701966-G-A

17450012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46701966-G-T

17450499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46702149-G-T

17450792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46702435-T-C

17451127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46702759-G-A

17451127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46702759-G-T

17452126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46703726-C-T

17452152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46703751-T-C

http://identifiers.org/hco/6/GRCh38#17452339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46703878-A-C

17452690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46704209-T-C

17452729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46704239-C-T

17452730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46704240-G-A

17452730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46704240-G-C

17452904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46704423-C-T

17452976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46704667-C-T

17453108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46704794-T-C

17453267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46704959-A-G

17453359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46705038-G-T

http://identifiers.org/hco/6/GRCh38#17453402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46705063-C-A

17453809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46705440-C-G

17453809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46705440-C-T

17456498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46706920-C-G

17457038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46707546-A-G

17457093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46707597-C-T

17457233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46707768-G-A

17457233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46707768-G-T

17457285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46707824-C-T

17457318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46707866-G-A

17457607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46708129-G-T

17457692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46708190-A-G

17458028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46708505-G-A

17458051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46708528-T-A

17458114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46708589-A-T

17458175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46708638-A-T

17458181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46708644-G-A

17458243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46708704-G-C

17458258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46708721-A-G

17458523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46708984-T-C

17458624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46709094-G-A

17458625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46709095-A-G

17458707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46709176-G-A

17458861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46709326-G-A

17458872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46709355-T-A

17458872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46709355-T-C

http://identifiers.org/hco/6/GRCh38#17459067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46709797-A-C

http://identifiers.org/hco/6/GRCh38#17462077-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46712536-A-C

17462395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46712871-C-T

17462433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46712944-A-G

17462505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46713419-C-T

17462709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46713620-A-G

17462847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46713819-G-A

17462847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46713819-G-T

17462877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46713848-G-C

17462877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46713848-G-T

http://identifiers.org/hco/6/GRCh38#17462914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46713884-C-A

17462914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46713884-C-T

17462916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46713886-A-G

17462916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46713886-A-T

http://identifiers.org/hco/6/GRCh38#17462936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46713917-A-C

17462936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46713917-A-G

17462998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 46713982-A-G

17462998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 46713982-A-T

http://identifiers.org/hco/6/GRCh38#17463070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46714054-C-A

17463070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 46714054-C-T

17463113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46714097-G-A

http://identifiers.org/hco/6/GRCh38#17463189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46714165-C-A

17464565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46715068-G-C

17464565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46715068-G-T

17464787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46715257-T-C

17464822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46715286-T-C

17465087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46715638-C-G

17465090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46715641-G-C

17465097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46715648-A-G

17466128-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46715985-T-G

http://identifiers.org/hco/6/GRCh38#17466132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46715989-A-C

http://identifiers.org/hco/6/GRCh38#17466430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46716262-C-A

17466497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46716305-C-T

17466534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46716342-C-T

17469753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46721273-A-G

17469770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46721290-G-A

17470508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46722305-G-A

17470508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46722305-G-C

17470692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46722494-G-A

http://identifiers.org/hco/6/GRCh38#17470815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46722617-A-C

17470953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46723057-T-C

17470953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46723057-T-G

17471029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46723126-A-G

17471029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46723126-A-T

17471140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46723235-T-G

17471205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46723299-T-A

http://identifiers.org/hco/6/GRCh38#17472643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46724539-A-C

17472643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46724539-A-G

17472672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46724568-C-T

17473148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46725042-G-C

17473445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46725387-G-A

http://identifiers.org/hco/6/GRCh38#17473662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46725602-C-A

17473736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46725675-C-T

17473847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46725786-T-C

17473904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46725835-A-G

17474138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46726126-G-T

17474182-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46726219-A-T

17474198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46726235-T-C

17474198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46726235-T-G

17474363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46726394-C-G

17474382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46726412-C-T

17474507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46726528-A-T

http://identifiers.org/hco/6/GRCh38#17474519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46726542-C-A

17474569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46726592-C-T

17474662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46727612-G-C

17474870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46727814-G-A

17475486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46728185-C-G

17476680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46736926-G-A

17479070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46737827-G-A

17479320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46738002-G-C

17479320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46738002-G-T

17479760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46738277-C-T

17479761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46738278-G-A

17479975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46738343-A-T

17480069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46738435-G-T

17480395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46738752-A-G

17480617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46738908-C-G

17480639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46738929-T-A

http://identifiers.org/hco/6/GRCh38#17481188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46739121-A-C

17481249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46739189-C-T

17482845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46739903-C-T

17482863-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46739921-T-A

17482875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46739933-G-A

17482875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46739933-G-C

17483084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46740124-G-A

17483237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46740252-C-G

17483574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46740570-C-T

17483589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46740584-T-G

17483694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46740696-C-T

17483836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46740793-A-G

17484168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46741119-C-T

17484314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46741282-T-C

17484629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46741609-G-A

17484629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46741609-G-C

17484933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46741880-T-C

http://identifiers.org/hco/6/GRCh38#17484970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46741917-C-A

http://identifiers.org/hco/6/GRCh38#17485105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46741992-A-C

17485196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46742119-G-A

http://identifiers.org/hco/6/GRCh38#17485309-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46742203-A-C

17485448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46742343-A-G

17485579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46742836-A-G

http://identifiers.org/hco/6/GRCh38#17485599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46742849-A-C

17485766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46742985-T-C

17485775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46742994-A-G

17485809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46743019-C-G

17485809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46743019-C-T

http://identifiers.org/hco/6/GRCh38#17485898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46743067-A-C

http://identifiers.org/hco/6/GRCh38#17485993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46743174-A-C

17485999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46743180-C-T

http://identifiers.org/hco/6/GRCh38#17488348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46745307-A-C

17488348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46745307-A-G

17488508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46745471-A-T

17488686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46745732-A-G

17488713-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46745757-A-T

17493275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46746545-A-G

17493366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46746642-T-C

http://identifiers.org/hco/6/GRCh38#17493380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46746656-C-A

17493380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 46746656-C-G

17493380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 46746656-C-T

http://identifiers.org/hco/6/GRCh38#17493381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46746657-C-A

17493381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 46746657-C-T

17493409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46746685-T-A

17493409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46746685-T-C

http://identifiers.org/hco/6/GRCh38#17493469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46746745-A-C

17493469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46746745-A-G

http://identifiers.org/hco/6/GRCh38#17493488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46746764-C-A

17493488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46746764-C-T

http://identifiers.org/hco/6/GRCh38#17493531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46746807-C-A

17496022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46751880-G-A

17496034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46751892-G-A

17496034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46751892-G-C

17496034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46751892-G-T

17496056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46751911-G-A

17496056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46751911-G-T

17496310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46752131-T-C

17496606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46752275-G-T

17496886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46752520-G-C

17497052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46752666-A-G

17497082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46752696-T-C

17497445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46753027-A-G

17497517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46753101-C-T

17497791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46753364-T-C

17497866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46753515-G-T

17498094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46753785-T-C

17498625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46754422-G-T

17501239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46758246-A-G

17501481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46758406-A-G

17501670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46758966-C-T

17501684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46758980-G-C

17501891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46759170-T-C

http://identifiers.org/hco/6/GRCh38#17501918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#46759188-A-C

17502026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46759316-C-T

17502226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46760398-G-A

17502437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46760600-T-C

17502473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46760637-T-C

17502717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46760873-A-G

17502849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46761006-A-G

17505155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46761445-A-G

17505292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46761576-G-C

17505354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46761638-T-C

http://identifiers.org/hco/6/GRCh38#17507009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#46762920-A-C

17507009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46762920-A-G

17507023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46762934-G-A

17507025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46762936-T-A

17507025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46762936-T-C

17507056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46762968-G-A

17507078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46762988-C-T

17507147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46763055-C-T

17507291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 46763194-T-C

17507294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 46763197-C-G

17507294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 46763197-C-T

17507390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46763276-T-G

http://identifiers.org/hco/6/GRCh38#17507450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#46763351-C-A

17507450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46763351-C-T

17507454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46763355-G-A

17507454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46763355-G-T

17507488-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46763385-T-A

http://identifiers.org/hco/6/GRCh38#17507531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#46763427-C-A

17507531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46763427-C-T

http://identifiers.org/hco/6/GRCh38#17507534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#46763434-C-A

17507541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46763439-G-T

17507547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46763445-G-A

17507547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46763445-G-T

17507554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46763450-C-T

http://identifiers.org/hco/6/GRCh38#17507746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#46763643-C-A

17507746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46763643-C-T

17507896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46764334-A-G

17507897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46764335-T-C

17507976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46764417-G-A

17508301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46764791-G-A

17508329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46764819-A-G

17508377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46764865-G-C

17508555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46765022-A-G

17508600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46765062-G-T

http://identifiers.org/hco/6/GRCh38#17508603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#46765065-C-A

17508614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46765076-C-T

17508647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46765109-T-C

17508657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46765121-C-T

17509152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46765272-A-G

17509210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46765327-A-G

17511275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46766339-G-A

17511334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46766372-G-T

http://identifiers.org/hco/6/GRCh38#17511409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#46766448-A-C

17511897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46766578-C-T

17511967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46766641-A-G

17511972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46766645-C-G

17512456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46766891-C-G

17512579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46766984-G-A

17512678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46767081-G-A

17512837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46767543-A-G

17513174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46768118-C-T

17513266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46768190-A-T

17513446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46768389-A-G

http://identifiers.org/hco/6/GRCh38#17513748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46768643-C-A

17513748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46768643-C-T

17513826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46768706-T-C

http://identifiers.org/hco/6/GRCh38#17513844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46768721-C-A

http://identifiers.org/hco/6/GRCh38#17513845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46768722-A-C

17513861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 46768738-T-C

17513965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46768842-G-A

17513982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46768859-G-T

17514010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46768898-C-T

17515817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46769805-C-T

17515899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46769881-T-C

17515911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46769893-C-G

17516315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46770435-T-C

17516382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46770507-T-G

17516829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46770771-T-C

17516865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46770809-T-G

17516884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46770828-G-A

17517018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46770902-G-A

17517018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46770902-G-C

17517018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46770902-G-T

17517215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46771093-G-T

http://identifiers.org/hco/6/GRCh38#17517282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46771152-C-A

17517428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46771302-C-G

17517475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46771347-A-G

17517938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46771693-G-A

17518077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46771827-G-A

17518246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46772429-T-C

17518334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46772517-A-G

17518383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46772564-G-A

17518959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46772947-C-T

17519157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46773132-G-A

17519157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46773132-G-C

17519157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46773132-G-T

17519159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46773134-G-A

17519242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46773221-G-A

17519375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46773380-A-G

17519391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46773396-A-G

17519545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46773541-G-A

17519671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46773666-G-A

17519671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46773666-G-T

17519804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46773779-T-C

17519873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46773809-A-G

17519873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46773809-A-T

17520007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46773916-T-C

http://identifiers.org/hco/6/GRCh38#17523084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46776144-A-C

http://identifiers.org/hco/6/GRCh38#17523185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46776250-A-C

http://identifiers.org/hco/6/GRCh38#17523245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46776299-A-C

17523269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46776324-A-G

17523332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46776388-T-C

17523359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46776410-G-A

17523475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46776472-G-A

17523645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46776606-A-G

17523681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46776632-G-A

17524103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46777354-A-T

17524173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46777425-G-T

http://identifiers.org/hco/6/GRCh38#17524264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46777525-C-A

17526465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46779647-G-T

17526531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46779699-G-C

http://identifiers.org/hco/6/GRCh38#17526652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46779815-A-C

17526700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46779860-G-A

17527137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46780135-A-G

17527520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46780534-A-G

17528673-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46781202-T-A

17529220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46781977-A-G

17529270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46782028-G-A

17529327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46782065-T-C

17529345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46782079-A-G

17529424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46782170-G-A

17529424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46782170-G-C

17529507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46782254-G-A

17529775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46782675-A-G

17529902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46782800-T-C

17530424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46782890-A-G

17530486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46782957-A-G

17530751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46783195-G-T

17531710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46783310-A-G

17532924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46783708-G-C

17533034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46783777-C-T

http://identifiers.org/hco/6/GRCh38#17533163-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46783871-A-C

17533165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46783873-G-A

17533191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46783899-A-G

17533211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46783915-A-G

17533227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46783939-A-G

17533398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46784119-A-G

17533536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46784283-T-C

http://identifiers.org/hco/6/GRCh38#17534624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46785342-C-A

17534753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46785442-T-G

17534918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46785614-T-G

17534927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46785623-C-G

17535793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46786923-C-G

17535793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46786923-C-T

http://identifiers.org/hco/6/GRCh38#17535887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46787047-A-C

17535920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46787079-C-T

http://identifiers.org/hco/6/GRCh38#17536146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46787261-A-C

17536146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46787261-A-G

17536287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46787381-A-G

17536448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46787534-G-A

17536572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46787651-A-G

17536767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46787781-G-A

17536810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46787824-C-T

17536811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46787825-G-A

17537035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46788094-T-C

17537036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46788095-T-G

17539038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46788925-T-A

17539125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46788992-G-A

17539125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46788992-G-T

17539133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46789000-G-A

17539133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46789000-G-C

17539133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46789000-G-T

http://identifiers.org/hco/6/GRCh38#17539219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46789051-C-A

17539288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 46789116-T-C

17539346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 46789174-G-A

17539346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 46789174-G-C

17539400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 46789228-T-C

17539400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 46789228-T-G

http://identifiers.org/hco/6/GRCh38#17539493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46789321-C-A

17539493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46789321-C-G

17539493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46789321-C-T

17539560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46789386-C-T

17539578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46789404-G-A

17539578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46789404-G-T

17539653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46789475-A-T

17540202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46789861-T-C

17541066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 46791415-C-G

17541981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46792519-G-T

17542311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46792798-C-G

http://identifiers.org/hco/6/GRCh38#17542390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46792877-A-C

17542567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46793030-G-C

17542698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46793156-G-C

17542698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46793156-G-T

17542734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46793194-A-G

17542900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 46793362-A-G

17542992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46793453-T-A

17543014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46793482-A-G

17543644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46793673-A-G

http://identifiers.org/hco/6/GRCh38#17543666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46793694-A-C

17544157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46794182-C-T

17544282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46794304-C-T

17544356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46794384-A-G

17544380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46794404-G-A

17549906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46796972-T-C

17549950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46797007-T-G

17550671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46799218-C-T

17550770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46799315-A-G

17550805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46799351-A-G

17551484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 46800022-A-G

17551635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: intron variant
orthologous variants: 46800176-T-C

17551670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: intron variant
orthologous variants: 46800210-T-C

17551670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: intron variant
orthologous variants: 46800210-T-G

17551672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: intron variant
orthologous variants: 46800212-G-T

17551675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: intron variant
orthologous variants: 46800215-T-A

17551675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: intron variant
orthologous variants: 46800215-T-C

17551675-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: intron variant
orthologous variants: 46800215-T-G

http://identifiers.org/hco/6/GRCh38#17551693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46800233-C-A

17551693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: intron variant
orthologous variants: 46800233-C-G

17551693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: intron variant
orthologous variants: 46800233-C-T

17556111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: intron variant
orthologous variants: 46801554-C-T

17556233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: intron variant
orthologous variants: 46801656-T-A

17556233-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: intron variant
orthologous variants: 46801656-T-G

http://identifiers.org/hco/6/GRCh38#17556256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46801680-C-A

17556266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: intron variant
orthologous variants: 46801690-A-G

17556453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3 prime UTR variant
orthologous variants: 46801850-G-C

17556453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3 prime UTR variant
orthologous variants: 46801850-G-T

http://identifiers.org/hco/6/GRCh38#17556504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46801893-C-A

17556570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3 prime UTR variant
orthologous variants: 46801962-A-G

http://identifiers.org/hco/6/GRCh38#17556767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46802147-C-A

17556906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3 prime UTR variant
orthologous variants: 46802270-T-C

http://identifiers.org/hco/6/GRCh38#17556915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46802279-C-A

17556934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3 prime UTR variant
orthologous variants: 46802298-G-A

http://identifiers.org/hco/6/GRCh38#17557098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46802439-C-A

17557098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3 prime UTR variant
orthologous variants: 46802439-C-T

17557216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3 prime UTR variant
orthologous variants: 46802573-G-C

http://identifiers.org/hco/6/GRCh38#17557313-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46802666-A-C

http://identifiers.org/hco/6/GRCh38#17557314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#46802667-C-A

17557350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3 prime UTR variant
orthologous variants: 46802709-T-C

17557434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3 prime UTR variant
orthologous variants: 46802774-G-A

17557434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3 prime UTR variant
orthologous variants: 46802774-G-T

17557462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3 prime UTR variant
orthologous variants: 46802796-T-G

17557621-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20039
most severe consequence: 3 prime UTR variant
orthologous variants: 46802955-T-A