32526099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: 3 prime UTR variant
orthologous variants: 114553247-A-G

32526116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114553231-T-C

http://identifiers.org/hco/3/GRCh38#32526126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114553221-C-A

32526196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114553153-C-T

http://identifiers.org/hco/3/GRCh38#32526210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114553139-C-A

http://identifiers.org/hco/3/GRCh38#32526230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114553122-C-A

32526230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114553122-C-T

32526444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114552948-G-A

32526444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114552948-G-T

32526504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114552890-T-C

http://identifiers.org/hco/3/GRCh38#32526676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114552555-C-A

32526688-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114552543-T-A

32526688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114552543-T-G

http://identifiers.org/hco/3/GRCh38#32526727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114552502-C-A

32526727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114552502-C-G

32526727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114552502-C-T

32526736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114552493-G-A

32526860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114552370-C-T

32528520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114550852-C-T

32528535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114550837-G-A

32528535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114550837-G-C

32528535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114550837-G-T

32528617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114550758-A-G

http://identifiers.org/hco/3/GRCh38#32528621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114550754-C-A

32528621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114550754-C-T

32528644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114550740-A-G

32529689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114549585-A-G

32529749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114549545-C-T

32529750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114549544-T-A

32529750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114549544-T-G

32529772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114549519-T-C

32529869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114549427-T-C

32529888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114549408-G-C

32529961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114549353-A-G

32529975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114549339-C-T

32530063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114549255-G-T

32530207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114549042-T-C

32530207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114549042-T-G

32530209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114549040-T-A

32530209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114549040-T-C

32530213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114549036-T-C

32530214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114549035-A-G

32530214-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114549035-A-T

32530269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114548985-A-G

32530331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 114548921-G-A

32530331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 114548921-G-T

32530362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114548900-G-A

32530362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114548900-G-T

32530374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114548888-A-T

http://identifiers.org/hco/3/GRCh38#32530420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114547030-C-A

32530420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114547030-C-G

http://identifiers.org/hco/3/GRCh38#32530525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114546924-A-C

32530580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114546867-T-C

32530750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114546801-G-C

32530750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114546801-G-T

32530751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114546800-T-A

32530832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114546763-A-T

32530835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114546760-T-A

http://identifiers.org/hco/3/GRCh38#32530864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114546740-C-A

32530864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114546740-C-T

http://identifiers.org/hco/3/GRCh38#32530893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114546712-A-C

32530893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114546712-A-G

32530933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114546673-T-A

32530955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114546651-G-T

http://identifiers.org/hco/3/GRCh38#32531030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114546583-C-A

32531030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114546583-C-T

32531097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114546544-G-A

32531097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114546544-G-T

32531111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114546530-C-T

32531170-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114546472-T-A

32531170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114546472-T-C

http://identifiers.org/hco/3/GRCh38#32531245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114546425-A-C

http://identifiers.org/hco/3/GRCh38#32531261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114546409-C-A

32531310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114546364-T-C

http://identifiers.org/hco/3/GRCh38#32531331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114546343-C-A

32531331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114546343-C-T

http://identifiers.org/hco/3/GRCh38#32531371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114546303-C-A

32531371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114546303-C-G

32531371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114546303-C-T

32531578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114545597-G-C

32531723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114545449-T-C

32531751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114545417-T-C

32532543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114545176-G-T

http://identifiers.org/hco/3/GRCh38#32532648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114545073-A-C

32532665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114545056-T-C

32532667-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114545054-T-A

32532680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114545041-A-G

32532700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114545021-G-A

32532705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114545016-T-C

32532707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114545014-T-C

32532728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114544994-A-G

32532728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114544994-A-T

32532884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114544869-G-T

32532899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114544852-G-T

32532989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114544774-T-C

32533039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114544724-A-G

32533147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114544618-T-C

32534472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114544328-T-C

32534480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114544320-G-C

32534480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114544320-G-T

32534483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114544317-A-G

http://identifiers.org/hco/3/GRCh38#32534514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114544292-A-C

32534656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114544151-A-G

http://identifiers.org/hco/3/GRCh38#32534663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114544144-A-C

http://identifiers.org/hco/3/GRCh38#32534698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114544117-C-A

32534731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114544082-T-C

32534779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114544035-T-C

32537040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114542640-T-A

32537040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114542640-T-C

32537846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114542142-A-G

32539284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-C

32539284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

32539391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

32540269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114540127-T-G

http://identifiers.org/hco/3/GRCh38#32540825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114538611-A-C

32540899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114538501-T-C

http://identifiers.org/hco/3/GRCh38#32540926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114538474-C-A

32540926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114538474-C-T

32540938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114538440-T-C

32540943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114538435-G-T

32541114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114538303-C-T

32541129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114538288-G-T

http://identifiers.org/hco/3/GRCh38#32541173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114538244-C-A

32541249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114538168-A-G

32541300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114538120-T-C

32541300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114538120-T-G

http://identifiers.org/hco/3/GRCh38#32544595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114535444-C-A

http://identifiers.org/hco/3/GRCh38#32544700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114535392-C-A

32545438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114534678-C-T

32545554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114534520-G-A

32545554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114534520-G-T

32545577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114534497-T-C

32545615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114534457-A-G

32545665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114534408-G-A

http://identifiers.org/hco/3/GRCh38#32545688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114534385-C-A

http://identifiers.org/hco/3/GRCh38#32545768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114534305-C-A

32545768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114534305-C-T

32545790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114534283-G-A

32545790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114534283-G-T

http://identifiers.org/hco/3/GRCh38#32546005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114534076-C-A

32548816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114530988-T-C

32548817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114530987-G-T

32548908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114530899-A-G

32549035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114530771-A-G

32549046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114530760-A-G

32558345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114528824-G-A

32558885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114527431-A-G

32559863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114526754-G-A

32559958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114526528-C-T

32560536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114526316-A-G

32561770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114525990-A-G

32562799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114523900-A-T

32562809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114523895-T-C

32562986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114523784-C-T

http://identifiers.org/hco/3/GRCh38#32563289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114523561-C-A

32563289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114523561-C-T

http://identifiers.org/hco/3/GRCh38#32563903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114523154-A-C

http://identifiers.org/hco/3/GRCh38#32563946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114523115-C-A

32563946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114523115-C-G

32564077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114523038-G-A

32564175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114522947-G-A

32564207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114522921-G-C

32564239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114522889-A-G

32564820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114522227-T-C

32567025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114522021-G-A

32567143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114521011-C-T

32567503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114520744-A-G

32568358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114520232-C-G

32568407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114520176-G-T

http://identifiers.org/hco/3/GRCh38#32568572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114520033-A-C

32568614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114519993-A-T

32568928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114519781-G-A

32568928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114519781-G-C

32568928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114519781-G-T

http://identifiers.org/hco/3/GRCh38#32569421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114519184-C-A

32569497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114519124-C-T

32569665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114518950-G-A

32569698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114518929-G-A

http://identifiers.org/hco/3/GRCh38#32569780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114518868-A-C

32570184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 114518470-G-A

32570184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 114518470-G-C

32570184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 114518470-G-T

32570271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114518395-G-A

32570271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114518395-G-T

32570331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114518363-G-A

32570331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114518363-G-C

32570331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114518363-G-T

32570333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114518361-A-G

32570334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114518360-G-A

32570334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114518360-G-C

32570334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114518360-G-T

32570534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 114518188-C-T

32570673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 114518045-C-T

http://identifiers.org/hco/3/GRCh38#32570693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#114518025-C-A

32570709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 114518009-T-C

32570809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 114517909-G-A

32570819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 114517896-G-A

32570819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18745
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 114517896-G-C