91140522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97371746-A-G

91140523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97371745-A-G

91140569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 97371697-G-A

91140615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97371651-T-C

91140787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97371502-T-C

http://identifiers.org/hco/12/GRCh38#91140809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97371482-C-A

91140866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97371425-G-A

91140866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97371425-G-T

91140997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97371316-A-G

91141009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97371304-G-A

91141009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97371304-G-C

http://identifiers.org/hco/12/GRCh38#91141011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97371302-C-A

91141011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97371302-C-T

91141018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97371295-T-C

91141070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97371243-G-A

91141070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97371243-G-T

91141116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97371197-C-T

91141160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97371154-A-G

91141188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97371126-G-A

http://identifiers.org/hco/12/GRCh38#91141189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97371125-C-A

91141189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97371125-C-T

91141722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97359998-T-C

91141759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97359961-T-C

91141764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97359956-C-T

91141766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97359954-G-T

http://identifiers.org/hco/12/GRCh38#91141767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97359953-C-A

91141767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97359953-C-T

http://identifiers.org/hco/12/GRCh38#91141769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97359951-C-A

http://identifiers.org/hco/12/GRCh38#91141773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97359947-C-A

91141773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97359947-C-T

91141793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97359931-G-T

http://identifiers.org/hco/12/GRCh38#91141863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97359876-C-A

91141890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97359849-A-G

91141958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97359776-T-C

http://identifiers.org/hco/12/GRCh38#91142036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97359696-C-A

91142044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97359688-T-A

91142044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97359688-T-C

91142047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97359685-T-C

91142232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97359535-T-A

91142232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97359535-T-C

91142241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97359526-C-T

91142324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97359450-C-T

91142396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97359378-T-C

91142483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97359289-C-T

91142544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97359224-A-G

http://identifiers.org/hco/12/GRCh38#91142613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97359008-C-A

91142656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97358921-G-A

91142656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97358921-G-T

91142703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97358894-A-G

91142726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97358871-G-A

91142726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97358871-G-C

91142782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97358834-A-G

91142852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97358765-T-C

91142862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97358756-A-G

91142930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97358692-C-T

91142981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97358643-A-G

91143031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97358581-T-A

91143031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97358581-T-C

91143092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97358518-G-T

91143096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97358514-G-A

91143120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97358498-G-A

http://identifiers.org/hco/12/GRCh38#91143129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97358489-C-A

91143129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97358489-C-T

91144097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97357240-G-A

91144097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97357240-G-T

http://identifiers.org/hco/12/GRCh38#91145021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97354504-C-A

91145033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97354492-A-G

91145046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97354479-A-G

91145194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3 prime UTR variant
orthologous variants: 97354333-A-T

91145317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 97354206-G-T

91145406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 97354117-G-A

91145448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 97354076-A-T

http://identifiers.org/hco/12/GRCh38#91145520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97354026-C-A

91145594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 97353957-G-A

91145594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 97353957-G-T

91145646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 97353905-T-C

91145697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 97353849-A-G

91145730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 97353816-T-C

91145752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97353814-A-G

91145757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97353809-T-C

91145887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97353707-T-C

91145924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97353670-T-C

91146045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97353526-G-T

91146134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 97353439-T-C

91146161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 97353412-C-T

91146248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 97353325-A-G

91151577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 97349663-G-C

91151577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 97349663-G-T

91151622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 97349626-T-A

91151622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 97349626-T-C

91151638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 97349613-A-G

91151639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 97349612-G-C

91151689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 97349562-C-G

91151736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 97349515-G-A

91151799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 97349452-C-T

91151853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97349399-T-C

91151854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97349398-G-T

91151876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97349382-G-A

91151879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97349379-A-T

91151883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97349375-C-G

91151883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97349375-C-T

91151948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97349312-G-A

91152055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97347838-G-T

91152114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97347776-T-C

91152218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97347684-A-G

91152487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97346470-T-C

http://identifiers.org/hco/12/GRCh38#91152526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97346433-C-A

91152526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97346433-C-T

91152947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97346050-A-G

91152987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97346019-G-T

91152993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97346013-T-C

http://identifiers.org/hco/12/GRCh38#91153016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97345985-C-A

91153016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97345985-C-T

91153017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97345984-A-G

91153129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 97345885-G-A

91153129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 97345885-G-T

91153269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97345750-A-G

91153270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97345749-T-C

http://identifiers.org/hco/12/GRCh38#91153272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97345747-C-A

91153272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97345747-C-T

91153274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97345745-A-G

91153274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97345745-A-T

91153415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97345612-C-T

http://identifiers.org/hco/12/GRCh38#91153426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97345601-C-A

91153674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97345331-T-G

91153759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97345243-T-C

http://identifiers.org/hco/12/GRCh38#91153770-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97345232-A-C

91153904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97345101-A-T

http://identifiers.org/hco/12/GRCh38#91154018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97344988-C-A

91154018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97344988-C-G

91154052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97344956-T-G

91154067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97344941-T-C

91155768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97344842-A-T

91155846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97344750-C-G

91156028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97344582-C-G

91156075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97344534-A-G

91156145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97344462-A-G

91156181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97344446-G-A

91156390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97344257-A-G

91156592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97344106-A-G

91156685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97344017-T-A

91156711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97343987-A-G

91156711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97343987-A-T

http://identifiers.org/hco/12/GRCh38#91156771-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97343934-A-C

91156979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97343779-C-T

http://identifiers.org/hco/12/GRCh38#91157001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97343757-C-A

91157058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97343693-G-T

91157131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 97343620-A-G

91157179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 97343572-G-A

91157195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 97343556-A-G

91157204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97343547-G-A

91157204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97343547-G-T

91157260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97343506-C-T

91157278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97343488-G-T

91157285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97343480-G-A

91157285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97343480-G-T

http://identifiers.org/hco/12/GRCh38#91157291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97343474-A-C

http://identifiers.org/hco/12/GRCh38#91157364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97343418-A-C

91157364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97343418-A-T

91157415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97343270-A-G

91157423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97343262-T-C

91157450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97343231-C-T

http://identifiers.org/hco/12/GRCh38#91157525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97343132-C-A

91157525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97343132-C-T

91157595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97343067-A-G

91157610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97343052-A-T

91157920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97342928-G-A

91157920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97342928-G-T

91158060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97342788-G-C

http://identifiers.org/hco/12/GRCh38#91158146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97342717-C-A

91158146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97342717-C-T

http://identifiers.org/hco/12/GRCh38#91158162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97342702-C-A

91158172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97342692-T-C

http://identifiers.org/hco/12/GRCh38#91158208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97342655-A-C

91158208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97342655-A-G

91158208-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97342655-A-T

http://identifiers.org/hco/12/GRCh38#91158448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97342414-A-C

91158510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant, splice_acceptor_variant
orthologous variants: 97342352-C-T

91158529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97342333-A-G

http://identifiers.org/hco/12/GRCh38#91158533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97342329-C-A

91158542-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97342321-T-A

91158542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97342321-T-C

91158665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97342193-C-T

91160315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97335428-C-T

91160380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97335360-A-G

91160592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97335184-T-C

91160688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97335090-G-C

91160721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97335057-G-A

91161256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97334072-C-T

91161440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97333885-T-C

91161551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97333767-C-G

91161678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97333578-C-T

91161689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97333566-G-C

91161695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97333560-T-G

91161713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97333542-T-G

91161876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97333351-C-T

91161910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97333320-A-G

91162161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97333235-G-A

91162382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97333093-A-G

91162427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97333047-A-G

91162540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97332921-C-T

91162633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97332849-T-C

91162663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97332812-A-G

91163073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97331961-A-G

http://identifiers.org/hco/12/GRCh38#91163226-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97331827-A-C

91163822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97331380-A-G

91163934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97331272-T-C

91163934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97331272-T-G

91164482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97331099-G-A

91164482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97331099-G-T

91164514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97331067-G-T

91164528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97331054-T-C

91164642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 97330937-A-G

91164729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97330850-G-A

91164729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97330850-G-T

91165138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97330004-T-C

91165250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97329895-G-T

91165475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97329700-G-T

91165713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97329283-G-T

91165716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97329280-T-C

91166003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97329011-A-G

91166380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97328634-T-C

91166690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97328318-A-G

91166723-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97328285-A-T

91166725-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97328283-A-T

91166826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97328185-T-C

91167005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97327947-A-G

91167231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97327711-A-G

91167558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97327415-C-T

91167736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97327193-A-G

91167816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97327118-A-G

91167818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97327116-T-C

91168710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97325487-T-A

91168911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97325301-G-A

http://identifiers.org/hco/12/GRCh38#91170213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97324288-A-C

91170343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97324174-C-G

91170343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97324174-C-T

91170381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97324136-A-G

91170704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97323788-G-A

91170721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97323771-G-A

91174634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97323103-T-C

91175248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97321323-A-G

91175504-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97321095-T-G

91177183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97320597-A-G

http://identifiers.org/hco/12/GRCh38#91177231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97320561-C-A

91177231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97320561-C-G

91177231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97320561-C-T

http://identifiers.org/hco/12/GRCh38#91177472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97320298-C-A

91177472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97320298-C-T

91177498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97320274-A-G

91177518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97320254-G-A

91177518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97320254-G-T

91177521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97320251-A-G

91177575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 97320196-G-C

91177597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 97320174-T-C

91177666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97320107-C-G

91177784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97320002-G-A

91177784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97320002-G-C

91177784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97320002-G-T

91177795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97319991-G-T

http://identifiers.org/hco/12/GRCh38#91177844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97319942-C-A

91177870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97319916-G-A

91177870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97319916-G-T

91177890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97319896-T-C

91177894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97319892-G-A

91178089-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97319669-T-A

91178089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97319669-T-C

91178154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97319605-G-A

91178205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 97319550-G-T

91178213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 97319542-T-C

91178282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 97319467-G-A

91178282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 97319467-G-C

91178283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 97319466-T-C

91178308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97319441-T-A

91178316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 97319433-G-A

91178316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 97319433-G-T

91178482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 97319293-A-G

91178513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 97319262-A-T

http://identifiers.org/hco/12/GRCh38#91178594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97319182-C-A

91178634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97319141-G-A

91178703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97319073-T-G

91178705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97319071-T-C

91178781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97318994-C-G

91178843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97318934-G-C

91178911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97318863-T-A

91179004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97318775-T-A

91179118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97318666-T-C

91179140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97318641-T-A

http://identifiers.org/hco/12/GRCh38#91179227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97318556-C-A

91179234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97318549-G-T

91179413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97318355-T-G

91179425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97318340-T-C

http://identifiers.org/hco/12/GRCh38#91179441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97318324-C-A

http://identifiers.org/hco/12/GRCh38#91179500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97318266-C-A

91179521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97318250-T-C

91179696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97318075-T-C

91179696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97318075-T-G

91180537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97317722-A-G

91180565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97317694-C-T

http://identifiers.org/hco/12/GRCh38#91180625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97317635-C-A

91180647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97317613-C-T

91180682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97317578-T-C

91180819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 97317462-A-G

91180831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 97317450-T-C

91180887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 97317389-G-A

91180946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 97317331-T-C

91181026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97317253-G-A

91181026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97317253-G-C

91181026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97317253-G-T

http://identifiers.org/hco/12/GRCh38#91181047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97317232-C-A

http://identifiers.org/hco/12/GRCh38#91181051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97317228-C-A

http://identifiers.org/hco/12/GRCh38#91181100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97317179-C-A

91181108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97317172-G-A

91181108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97317172-G-T

91181356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97316959-G-A

91181370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97316945-T-C

91181386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97316930-C-T

http://identifiers.org/hco/12/GRCh38#91181483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97316805-A-C

91181688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97316637-C-T

91181843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97316500-C-G

http://identifiers.org/hco/12/GRCh38#91181896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97316439-C-A

91181915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97316422-C-T

91181990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97316332-A-T

91182037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97316280-A-T

91182065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97316253-A-G

91182109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97316212-A-G

91182128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97316193-T-C

http://identifiers.org/hco/12/GRCh38#91182252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97316077-C-A

91182333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97315994-A-G

http://identifiers.org/hco/12/GRCh38#91182535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97315769-A-C

91182579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97315725-A-G

91182758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 97315543-G-T

91183098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2705
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 97315197-T-C