http://identifiers.org/hco/17/GRCh38#76004777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116109682-C-A

76004777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116109682-C-G

76004784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116109689-T-C

76004902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116109795-T-A

76005153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116109993-A-G

76005275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116110457-T-C

76005326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116110508-G-A

76005336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116110518-C-G

76005338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116110520-A-G

76005375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116110554-G-T

76005379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116110558-T-C

76005379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116110558-T-G

http://identifiers.org/hco/17/GRCh38#76005409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116110588-C-A

76005409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116110588-C-G

76005409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 116110588-C-T

http://identifiers.org/hco/17/GRCh38#76005468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116110638-C-A

76005468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116110638-C-T

76005572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116110706-G-A

76005572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116110706-G-T

http://identifiers.org/hco/17/GRCh38#76005637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#116110769-A-C

76005637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 116110769-A-T

http://identifiers.org/hco/17/GRCh38#76005685-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#116110816-A-C

76005685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 116110816-A-G

http://identifiers.org/hco/17/GRCh38#76005726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116110854-C-A

76005726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116110854-C-T

76005901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116111013-G-T

http://identifiers.org/hco/17/GRCh38#76005926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#116111044-C-A

http://identifiers.org/hco/17/GRCh38#76005994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116111109-C-A

76005994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116111109-C-G

76005997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116111112-G-A

76005997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116111112-G-C

76005997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116111112-G-T

http://identifiers.org/hco/17/GRCh38#76005998-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116111113-A-C

76005998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116111113-A-G

76006000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron variant
orthologous variants: 116111115-T-A

76006000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron variant
orthologous variants: 116111115-T-C

76006000-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron variant
orthologous variants: 116111115-T-G

76006017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron variant
orthologous variants: 116111133-T-C

76006063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron variant
orthologous variants: 116111178-G-T

http://identifiers.org/hco/17/GRCh38#76006753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116111301-C-A

76006758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron variant
orthologous variants: 116111306-A-G

http://identifiers.org/hco/17/GRCh38#76006759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116111307-A-C

76006759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron variant
orthologous variants: 116111307-A-G

76006809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron variant
orthologous variants: 116111357-T-A

76006809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron variant
orthologous variants: 116111357-T-C

http://identifiers.org/hco/17/GRCh38#76006853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116111387-A-C

76006853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 116111387-A-G

76006853-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 116111387-A-T

76006862-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 116111396-T-A

76006862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 116111396-T-C

76006862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 116111396-T-G

76006882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 116111416-G-A

76006904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 116111434-G-A

76007043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 116111541-A-T

http://identifiers.org/hco/17/GRCh38#76007059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116111557-C-A

76007059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, splice_donor_variant
orthologous variants: 116111557-C-T

76007096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116111574-G-A

76007096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116111574-G-C

76007096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116111574-G-T

76007098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 116111576-C-T

76007117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116111598-G-A

76007117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116111598-G-C

76007117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116111598-G-T

http://identifiers.org/hco/17/GRCh38#76007118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116111599-C-A

76007118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116111599-C-T

76007138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116111619-A-G

76007162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116111643-G-A

76007162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116111643-G-C

76007162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116111643-G-T

76007256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116111737-T-C

76007310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116111791-A-G

76007310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116111791-A-T

76007322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116111803-G-A

76007322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116111803-G-C

76007478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116111959-G-A

76007478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116111959-G-T

76007511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116111992-G-A

76007559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116112040-C-G

76007559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116112040-C-T

76007832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116112313-G-A

76007982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116112463-G-T

76008066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116112547-G-A

76008105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116112586-G-A

76008105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 116112586-G-T

76008123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116112604-C-G

76008123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116112604-C-T

76008126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116112607-C-G

76008126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116112607-C-T

http://identifiers.org/hco/17/GRCh38#76008301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116112782-C-A

76008301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116112782-C-G

76008301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116112782-C-T

76008305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116112786-G-A

76008305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116112786-G-C

76008305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116112786-G-T

76008353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116112834-T-C

76008442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116112923-G-A

76008442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116112923-G-T

http://identifiers.org/hco/17/GRCh38#76008470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116112951-A-C

76008470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116112951-A-T

http://identifiers.org/hco/17/GRCh38#76008547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116113028-C-A

76008547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116113028-C-T

http://identifiers.org/hco/17/GRCh38#76008603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116113084-A-C

76008687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116113168-A-G

76008732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116113213-C-T

76008894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116113375-C-T

76008903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116113384-G-A

76008903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116113384-G-C

76008903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116113384-G-T

76008963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116113444-G-A

76008963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116113444-G-T

76009037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116113518-G-A

76009149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116113630-G-A

76009149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 116113630-G-C

76009149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 116113630-G-T

76009172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116113653-G-A

76009172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116113653-G-T

76009177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116113658-T-C

76009215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116113696-T-C

76009215-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116113696-T-G

76009245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116113726-G-A

76009245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116113726-G-C

76009245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116113726-G-T

76009311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116113792-G-A

http://identifiers.org/hco/17/GRCh38#76009446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116113927-C-A

76009446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116113927-C-G

76009446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116113927-C-T

76009473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116113954-C-T

http://identifiers.org/hco/17/GRCh38#76009529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116114010-C-A

76009529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116114010-C-T

76009605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116114086-G-A

76009608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116114089-G-T

http://identifiers.org/hco/17/GRCh38#76009644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116114125-C-A

76009644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116114125-C-T

76009668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116114149-C-T

76009878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116114359-C-T

http://identifiers.org/hco/17/GRCh38#76010247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116114728-C-A

76010403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116114884-C-T

http://identifiers.org/hco/17/GRCh38#76010450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116114931-C-A

76010450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116114931-C-T

76010484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116114968-A-G

76010569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116115059-A-T

76010599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116115091-T-C

http://identifiers.org/hco/17/GRCh38#76010637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116115139-A-C

76010637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116115139-A-G

http://identifiers.org/hco/17/GRCh38#76010646-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116115148-A-C

76010666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116115168-G-T

http://identifiers.org/hco/17/GRCh38#76010674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116115176-C-A

76010674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116115176-C-G

76010674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116115176-C-T

76010683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116115185-C-T

76010897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116115292-C-G

76011241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116115585-G-A

76011254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116115598-G-A

76011309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116115644-C-T

76011449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116115762-G-T

76011460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116115772-G-A

76011460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116115772-G-T

76011489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116115804-G-A

76011489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116115804-G-T

76011508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116115824-G-A

76011508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116115824-G-T

76011509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116115825-G-A

76011509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116115825-G-T

76011519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116115835-G-T

76011522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116115838-C-T

76011542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116115860-T-C

76011543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116115861-A-G

76011548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116115866-G-T

76011563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116115881-G-A

76011614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116115932-G-A

76011617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116115935-G-A

76011689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116116005-G-A

76011739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116116055-A-G

76011809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116116125-G-T

76011823-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116116139-T-A

76011823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116116139-T-C

76011838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116116154-G-A

76011894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116116210-G-A

76011922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116116222-G-A

76011957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116116259-G-A

http://identifiers.org/hco/17/GRCh38#76012087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116116391-C-A

76012087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 116116391-C-G

76012087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 116116391-C-T

http://identifiers.org/hco/17/GRCh38#76012104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116116408-C-A

76012113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116116418-A-G

76012117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116116422-G-A

76012117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116116422-G-T

http://identifiers.org/hco/17/GRCh38#76012144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116116440-C-A

76012144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116116440-C-G

76012144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116116440-C-T

http://identifiers.org/hco/17/GRCh38#76012149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116116445-C-A

76012149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116116445-C-T

http://identifiers.org/hco/17/GRCh38#76012155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116116451-A-C

76012155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116116451-A-G

76012155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116116451-A-T

http://identifiers.org/hco/17/GRCh38#76014566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116117955-C-A

76014604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116117993-G-A

http://identifiers.org/hco/17/GRCh38#76014605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#116117994-A-C

76014605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116117994-A-G

76014653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116118077-G-T

76014660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116118084-T-C

76014671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116118124-G-T

http://identifiers.org/hco/17/GRCh38#76014686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116118136-C-A

76014686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116118136-C-G

76014692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116118142-G-A

76014692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116118142-G-T

76014694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116118144-C-T

76014726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116118186-G-C

76014756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116118235-C-T

76014798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116118306-G-A

76014798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116118306-G-T

76014817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116118325-A-G

76014817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116118325-A-T

http://identifiers.org/hco/17/GRCh38#76014820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116118328-C-A

76014820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116118328-C-G

76014820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116118328-C-T

76014852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116118345-G-T

76014939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116118407-G-A

76014939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116118407-G-T

76014942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116118410-G-A

76014942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116118410-G-T

76014974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116118442-G-A

76014974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116118442-G-T

76015041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116118509-C-T

http://identifiers.org/hco/17/GRCh38#76015101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116118569-C-A

76015101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116118569-C-T

76015108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 116118576-C-T

76015116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116118584-G-A

76015116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116118584-G-T

76015120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116118588-A-G

76015121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116118589-G-T

76015127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116118595-G-A

76015137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116118605-A-G

http://identifiers.org/hco/17/GRCh38#76015142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#116118610-C-A

76015142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116118610-C-G

76015142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116118610-C-T

76015154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116118625-G-T

76015184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116118638-G-A

76015184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116118638-G-T

76015185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116118639-C-G

76015185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116118639-C-T

http://identifiers.org/hco/17/GRCh38#76015193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116118647-C-A

76015193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116118647-C-T

http://identifiers.org/hco/17/GRCh38#76015199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116118653-C-A

76015298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116118739-C-T

76015370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116118811-C-G

76015370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116118811-C-T

http://identifiers.org/hco/17/GRCh38#76015381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116118821-C-A

76015381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116118821-C-T

http://identifiers.org/hco/17/GRCh38#76015389-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116118829-A-C

76015389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116118829-A-G

76015389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116118829-A-T

76015530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116118965-G-A

76015596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116119031-C-G

76015596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116119031-C-T

76015597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116119032-G-A

76015597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116119032-G-C

http://identifiers.org/hco/17/GRCh38#76015671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116119095-C-A

76015671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116119095-C-T

76015855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116119257-T-C

http://identifiers.org/hco/17/GRCh38#76015859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116119261-A-C

76017451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116119995-C-T

76017478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116120031-A-G

76017511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116120055-T-C

http://identifiers.org/hco/17/GRCh38#76017597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116120140-C-A

76017597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116120140-C-T

http://identifiers.org/hco/17/GRCh38#76017607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116120150-C-A

76017607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116120150-C-T

http://identifiers.org/hco/17/GRCh38#76017641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116120159-C-A

76017641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116120159-C-G

76017641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116120159-C-T

76017680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116120167-G-A

76017680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116120167-G-T

76017711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116120201-C-T

76017722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116120210-T-C

http://identifiers.org/hco/17/GRCh38#76017755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116120243-C-A

76017755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116120243-C-T

76017823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116120311-C-G

http://identifiers.org/hco/17/GRCh38#76017834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/11/GRCm39#116120322-C-A

76017872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116120360-T-A

76017878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116120366-G-A

76017891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116120379-C-T

76017907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116120395-T-C

76017907-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116120395-T-G

76017911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 116120399-G-A

76017930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116120418-G-A

76017964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116120440-T-A

76017964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116120440-T-G

76018018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116120476-A-G

76018018-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116120476-A-T

http://identifiers.org/hco/17/GRCh38#76018069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116120528-C-A

76018069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116120528-C-G

76018155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116120565-G-T

76018281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116120684-G-A

76018281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116120684-G-T

http://identifiers.org/hco/17/GRCh38#76018284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116120687-A-C

76018284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116120687-A-T

76018300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116120708-C-T

76018316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116120724-G-A

76018316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116120724-G-T

http://identifiers.org/hco/17/GRCh38#76018317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116120725-C-A

http://identifiers.org/hco/17/GRCh38#76018318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116120726-C-A

76018318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116120726-C-T

76018391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116120783-A-G

76018566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116120915-A-G

76018570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116120919-G-A

76018587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116120936-T-A

76018587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116120936-T-C

http://identifiers.org/hco/17/GRCh38#76018642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116120985-C-A

76018642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116120985-C-G

76018642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116120985-C-T

76018690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116121021-G-T

76018714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116121048-A-G

76018714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116121048-A-T

76018784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116121127-A-G

76018825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116121160-G-A

76018825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116121160-G-T

76018826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116121161-G-A

76018826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116121161-G-T

76018868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116121213-T-G

http://identifiers.org/hco/17/GRCh38#76018872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116121217-C-A

76018872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116121217-C-G

76018872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116121217-C-T

76018903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116121231-G-A

http://identifiers.org/hco/17/GRCh38#76019071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116121399-C-A

76019071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116121399-C-G

76019071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116121399-C-T

76019076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116121404-G-A

76019076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116121404-G-T

http://identifiers.org/hco/17/GRCh38#76019110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116121437-C-A

76019110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116121437-C-T

http://identifiers.org/hco/17/GRCh38#76019120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116121447-C-A

76019120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116121447-C-T

76019200-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116121505-T-A

76019200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116121505-T-C

76019326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116121615-C-G

http://identifiers.org/hco/17/GRCh38#76019391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116121658-A-C

76019391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116121658-A-G

76019436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116121680-T-C

76019494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116121712-G-T

http://identifiers.org/hco/17/GRCh38#76019510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116121728-C-A

76019510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116121728-C-T

http://identifiers.org/hco/17/GRCh38#76019540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116121756-C-A

76019540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116121756-C-T

http://identifiers.org/hco/17/GRCh38#76019561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116121777-A-C

76019577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116121793-G-A

76019577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116121793-G-T

76019795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116122036-G-A

76019795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116122036-G-T

76021407-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116123151-T-A

76021447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116123193-G-A

http://identifiers.org/hco/17/GRCh38#76021501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116123253-C-A

http://identifiers.org/hco/17/GRCh38#76021648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116123402-C-A

76021648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116123402-C-T

76021722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116123504-G-A

76021722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116123504-G-T

http://identifiers.org/hco/17/GRCh38#76021770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116123552-C-A

76021770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116123552-C-T

76021781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 116123563-G-A

76021781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 116123563-G-T

76021785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116123567-G-A

76021785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116123567-G-T

76021800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116123582-G-T

http://identifiers.org/hco/17/GRCh38#76021805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116123585-C-A

76021805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116123585-C-T

http://identifiers.org/hco/17/GRCh38#76021833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116123613-C-A

76021833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116123613-C-T

76021930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116123714-G-A

76021930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116123714-G-T

76022069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116123829-A-G

76022103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116123857-G-A

76022103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116123857-G-T

http://identifiers.org/hco/17/GRCh38#76022112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116123864-C-A

76022112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116123864-C-T

76022118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116123870-C-G

76022269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116123995-G-A

76022269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116123995-G-T

76022379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116124194-G-C

76022379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116124194-G-T

76022426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 116124225-C-T

76022443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 116124242-A-G

http://identifiers.org/hco/17/GRCh38#76022576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116124379-C-A

76022576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116124379-C-G

76022576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116124379-C-T

76022605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116124408-T-C

http://identifiers.org/hco/17/GRCh38#76022608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116124413-C-A

http://identifiers.org/hco/17/GRCh38#76022684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116124498-C-A

76022684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116124498-C-T

76022689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116124503-C-T

76023143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116124851-T-C

76023144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116124852-G-A

76023144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116124852-G-T

http://identifiers.org/hco/17/GRCh38#76023311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116125000-C-A

76023311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116125000-C-T

76023340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116125029-G-A

76023343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116125032-G-A

76023406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116125095-C-G

76023406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116125095-C-T

76023488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116125175-A-G

76023583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116125278-A-G

76023619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116125314-C-T

http://identifiers.org/hco/17/GRCh38#76023640-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116125335-A-C

76023675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116125367-G-A

76023677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116125369-C-T

76023754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116125462-T-A

76023754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116125462-T-C

http://identifiers.org/hco/17/GRCh38#76023760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116125468-C-A

76023760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116125468-C-T

http://identifiers.org/hco/17/GRCh38#76023778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116125484-C-A

76023778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116125484-C-G

76023778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116125484-C-T

http://identifiers.org/hco/17/GRCh38#76023797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116125497-C-A

76023797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116125497-C-G

76023807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116125507-G-A

http://identifiers.org/hco/17/GRCh38#76023870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116125603-C-A

76023870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116125603-C-T

http://identifiers.org/hco/17/GRCh38#76023871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116125604-C-A

76023871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116125604-C-G

76023871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116125604-C-T

76023882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116125615-G-A

76023882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116125615-G-T

76023911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116125642-G-A

76023911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116125642-G-C

76023911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116125642-G-T

76023914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116125664-C-G

76023914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116125664-C-T

76023953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116125703-G-A

http://identifiers.org/hco/17/GRCh38#76023967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116125718-C-A

76023967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116125718-C-T

76024014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116125751-G-A

76024014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116125751-G-C

76024014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116125751-G-T

http://identifiers.org/hco/17/GRCh38#76024175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116125910-C-A

76024199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116125935-C-T

http://identifiers.org/hco/17/GRCh38#76024203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116125939-C-A

76024203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116125939-C-T

http://identifiers.org/hco/17/GRCh38#76024210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116125946-A-C

76024210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116125946-A-G

http://identifiers.org/hco/17/GRCh38#76024225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116125960-C-A

76024225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116125960-C-T

76024293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116126006-G-A

http://identifiers.org/hco/17/GRCh38#76024370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116126077-C-A

76024370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116126077-C-T

76024454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116126125-C-T

76024467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116126137-G-A

76024588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116126267-T-C

76024780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116126393-G-A

76024828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116126432-C-T

76025270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116127657-G-A

76025303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116127688-C-T

76025363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116127748-C-T

76025594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116127946-T-G

76025714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116128048-G-A

76025913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116128237-G-A

76025927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116128247-G-A

76026534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116128271-A-G

76026628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116128358-C-T

76026765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116128482-C-G

76026765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116128482-C-T

76026835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116128507-T-C

http://identifiers.org/hco/17/GRCh38#76027047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#116128680-C-A

76027047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116128680-C-T

76027257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 116128871-G-A

76027257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3503
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 116128871-G-T