51817778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: 7242776-T-A

51817823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: 7242732-G-C

51817823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: 7242732-G-T

51817827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: 7242728-C-T

51817851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: 7242704-G-C

51817851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: 7242704-G-T

51817891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: 7242664-G-A

51818022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: 7242327-T-G

51818102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: 7242262-A-G

51818133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: 7242232-C-T

http://identifiers.org/hco/8/GRCh38#51818186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7242183-C-A

http://identifiers.org/hco/8/GRCh38#51818336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7242038-C-A

51818469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: 7241893-A-G

51818469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: 7241893-A-T

51818492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: 7241870-G-A

51818492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: 7241870-G-T

http://identifiers.org/hco/8/GRCh38#51818536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7241831-A-C

51818536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: 7241831-A-G

51818668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: 7241626-T-C

http://identifiers.org/hco/8/GRCh38#51818699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7241607-A-C

http://identifiers.org/hco/8/GRCh38#51818718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7241588-C-A

http://identifiers.org/hco/8/GRCh38#51818729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7241577-C-A

51818859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: 7241472-A-T

51818906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: 7241444-A-G

51818931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: 7241420-G-A

51819202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: 7241182-A-G

51819211-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: 7241173-A-T

51819255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: 7241130-A-G

51819472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: 7240921-G-A

http://identifiers.org/hco/8/GRCh38#51819475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7240918-C-A

51819497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: 7240899-C-T

51819774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: 7240630-A-G

51819853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: 7240554-G-A

51819853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: 7240554-G-T

http://identifiers.org/hco/8/GRCh38#51819891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7240539-C-A

51820294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 7240159-T-C

51820367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7240088-T-C

51820466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7239989-T-C

51820712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7239743-C-T

51820800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7239699-T-C

51826675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7237969-G-A

51826794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7237808-T-C

51826795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7237807-G-A

51826795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7237807-G-T

51826826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7237778-T-C

51826969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7237608-T-C

51826971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7237606-C-G

51826971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7237606-C-T

51826986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7237591-A-G

51827002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7237575-T-A

51827002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7237575-T-C

51827093-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7237504-A-T

51827148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7237458-G-A

51827148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7237458-G-C

51827148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7237458-G-T

51828954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7236281-C-T

51829016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7236218-T-C

51829278-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7236001-T-A

51829326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7235956-A-G

51829326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7235956-A-T

51829397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7235900-G-A

51829504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7235781-G-T

51829875-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7235425-T-A

51830207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7235145-A-G

51830277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7235068-C-T

51830355-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7234984-T-G

http://identifiers.org/hco/8/GRCh38#51831319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7233699-A-C

51831319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7233699-A-G

51831319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7233699-A-T

51831339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7233679-T-C

51831658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7233403-T-C

51831694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7233377-G-A

51831776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7232526-C-T

51831787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7232515-T-C

http://identifiers.org/hco/8/GRCh38#51833383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7231408-C-A

51833505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7231297-G-C

51833505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7231297-G-T

51833636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7231167-G-T

51833669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7231134-G-A

51833754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7231048-A-G

51833754-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7231048-A-T

51833868-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7230937-A-T

51834421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7230700-A-G

51834421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7230700-A-T

51834474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7230644-A-T

51834826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7230210-C-T

51835108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7229673-C-T

51835969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7228590-C-T

51835999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7228554-G-C

51835999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7228554-G-T

51836019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7228534-C-T

51836147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7228398-G-C

51836188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7228362-G-T

51836291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7228275-T-C

51836502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7228013-T-C

51836505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7228010-G-C

51836749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7227481-T-G

51836839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7227407-G-A

51836856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7227390-G-A

51836949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7227306-T-C

51836949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7227306-T-G

51836959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7227302-T-C

51838534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7226345-A-G

51838613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7226254-T-A

51838909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7225975-A-G

51838942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7225951-A-G

51838978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7225912-A-G

51839002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7225896-G-A

51839179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7225732-T-C

51839240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7225682-T-G

51839317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7225622-A-G

http://identifiers.org/hco/8/GRCh38#51839348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7225591-C-A

51839348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7225591-C-T

http://identifiers.org/hco/8/GRCh38#51839541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7225399-C-A

51839541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7225399-C-T

51840238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7224718-G-A

51840407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7224373-T-C

51841052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7223727-G-T

51841108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7223677-T-A

51841563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7223237-A-G

51841678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7223118-A-G

51843672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7219918-G-A

51843733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7219868-C-G

51843736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7219866-G-A

51843782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7219843-T-C

51843955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7219689-A-G

51844184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7219472-T-G

51844459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7219048-C-G

51844492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7219017-T-C

51844492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7219017-T-G

51844785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7218769-C-T

http://identifiers.org/hco/8/GRCh38#51844804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7218758-C-A

51844804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7218758-C-T

51844848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7218715-C-T

51844849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7218714-C-T

51844868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7218692-T-C

51844873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7218687-G-T

http://identifiers.org/hco/8/GRCh38#51844950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7218609-A-C

51844954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7218605-G-T

http://identifiers.org/hco/8/GRCh38#51844958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7218601-C-A

51845021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7218537-T-A

51845021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7218537-T-C

51845021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7218537-T-G

51845090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7218450-G-A

51845090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7218450-G-T

http://identifiers.org/hco/8/GRCh38#51845093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7218447-A-C

51845093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7218447-A-G

http://identifiers.org/hco/8/GRCh38#51845126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7218415-C-A

51845126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7218415-C-G

51845134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7218407-A-G

51845145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7218400-G-A

51845145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7218400-G-C

51845145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7218400-G-T

51845232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7218315-T-C

51845272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7218285-G-T

51845325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7218237-T-C

http://identifiers.org/hco/8/GRCh38#51845357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7218206-C-A

51845357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7218206-C-T

http://identifiers.org/hco/8/GRCh38#51845475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7218114-A-C

51845475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7218114-A-G

http://identifiers.org/hco/8/GRCh38#51845476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7218113-C-A

51845476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7218113-C-T

51845590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7218032-G-C

51845590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7218032-G-T

http://identifiers.org/hco/8/GRCh38#51845622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7218000-A-C

51845622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7218000-A-G

51845622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7218000-A-T

http://identifiers.org/hco/8/GRCh38#51846023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7217633-C-A

51846111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7217550-T-A

51846357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7217241-C-T

51848461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7215728-T-A

51848828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7214792-T-G

51849517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7213154-T-C

51849546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7213128-T-C

51849709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7212984-A-G

51849711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7212982-T-C

http://identifiers.org/hco/8/GRCh38#51849812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7212893-C-A

51849812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7212893-C-T

51849816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7212889-A-G

51849948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7212762-C-T

51849986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7212725-G-C

51850064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 7212648-T-C

51850204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7212518-A-G

51850316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7212431-T-C

51850438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7212324-T-C

51850527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7212110-A-G

51851080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7211518-T-G

51851124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7211475-C-T

http://identifiers.org/hco/8/GRCh38#51851146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#7211453-C-A

51851146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7211453-C-T

http://identifiers.org/hco/8/GRCh38#51851181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7211420-A-C

51852494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7210707-G-T

51852646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7210549-C-T

51852769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7210430-T-C

51852769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7210430-T-G

51852784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7210415-T-C

51853323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7209490-C-T

51853331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7209483-T-C

51853365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7209449-A-G

51853480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7209334-T-A

51854039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7208575-T-C

51857036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7207384-G-C

51857106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7207310-G-A

http://identifiers.org/hco/8/GRCh38#51857580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7206341-C-A

51857804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7206138-A-G

51860607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7191067-T-C

http://identifiers.org/hco/8/GRCh38#51860713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7190968-A-C

51860713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7190968-A-G

http://identifiers.org/hco/8/GRCh38#51860775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7190907-C-A

http://identifiers.org/hco/8/GRCh38#51861182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7190500-A-C

51861263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7190401-A-G

51861641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7190106-C-G

51861653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7190094-T-G

51862262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7189718-C-T

51862326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7189648-A-G

51863099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7187619-T-G

51863284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7187423-A-G

http://identifiers.org/hco/8/GRCh38#51868197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7178732-C-A

51868530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7178460-T-A

51868533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7178457-G-T

51868986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7176762-A-G

http://identifiers.org/hco/8/GRCh38#51869024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7176723-A-C

51869024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7176723-A-G

51869144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7176635-C-T

51869164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7176615-G-A

51869295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7176527-A-G

51869382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7176456-C-T

51869453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7176397-C-T

51869689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7176151-G-A

51894132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7164044-A-G

51894259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7163920-C-G

51894599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7163689-C-T

51894651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7163592-A-T

51894816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7162524-G-T

51894936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7162414-A-G

http://identifiers.org/hco/8/GRCh38#51895083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#7162274-A-C

51895225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7162160-G-A

51896858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7160811-T-C

51897383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7160428-T-C

51897993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7159772-G-A

51898236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7159549-T-C

51898269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30483
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7159516-T-C