132196379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: 110769241-G-A

132196379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: 110769241-G-T

132196451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: 110769172-A-G

http://identifiers.org/hco/12/GRCh38#132196500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110769128-C-A

132196500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: 110769128-C-T

132196566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: 110769085-A-G

132196577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: 110769071-G-C

132196643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: 110769017-G-A

132196643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: 110769017-G-T

132196649-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: 110769011-T-G

http://identifiers.org/hco/12/GRCh38#132196663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110769000-A-C

132196663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: 110769000-A-G

http://identifiers.org/hco/12/GRCh38#132196675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110768988-C-A

132196675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: 110768988-C-T

132196686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: 110768972-G-A

132196686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: 110768972-G-C

132196686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: 110768972-G-T

http://identifiers.org/hco/12/GRCh38#132196697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110768961-C-A

132196697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: 110768961-C-T

132196706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: 110768945-T-G

http://identifiers.org/hco/12/GRCh38#132196714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110768937-C-A

132196714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: 110768937-C-G

132196714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: 110768937-C-T

132196723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: 110768928-G-T

132196783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: 110768866-G-A

132196783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: 110768866-G-C

132196951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: 110768679-G-C

132196951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: 110768679-G-T

http://identifiers.org/hco/12/GRCh38#132196960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110768670-C-A

132196960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: 110768670-C-T

132196993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: 110768650-G-A

http://identifiers.org/hco/12/GRCh38#132196994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110768649-C-A

132196994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: 110768649-C-T

132197084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: 110768541-T-C

132197084-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 3 prime UTR variant
orthologous variants: 110768541-T-G

132197114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: missense variant
orthologous variants: 110768511-C-T

132197225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: missense variant
orthologous variants: 110768400-C-T

132197268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron variant
orthologous variants: 110768358-A-G

http://identifiers.org/hco/12/GRCh38#132197272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110768354-C-A

http://identifiers.org/hco/12/GRCh38#132197779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110767209-C-A

132197779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron variant
orthologous variants: 110767209-C-T

132197904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: missense variant
orthologous variants: 110767084-G-A

132197904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: missense variant
orthologous variants: 110767084-G-T

http://identifiers.org/hco/12/GRCh38#132197972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110767019-C-A

132199287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110765687-A-G

132199288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110765686-G-T

132199296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110765678-T-C

132199311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110765653-G-A

132199311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110765653-G-C

132199311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110765653-G-T

132199376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110765513-G-A

132199376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110765513-G-C

132199376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110765513-G-T

132199379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110765510-G-T

132199632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110765252-G-A

132199671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110765217-C-T

132199754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110765142-C-G

132199754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110765142-C-T

http://identifiers.org/hco/12/GRCh38#132199790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110765106-C-A

132199790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110765106-C-T

132200143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110764801-G-C

132200292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110764584-A-G

132200362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110764502-G-A

132200362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110764502-G-T

132200409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110764451-A-G

http://identifiers.org/hco/12/GRCh38#132200417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110764444-C-A

132200417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110764444-C-T

132200420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110764441-T-G

132200421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110764440-G-T

132200513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110764290-T-C

132200535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110764267-C-T

132200632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110764162-G-A

132200632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110764162-G-T

132200647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110764147-C-G

132200647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110764147-C-T

132200711-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110764091-T-A

132200711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110764091-T-G

132200750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110764046-G-A

132200772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110764011-G-A

132200772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110764011-G-T

http://identifiers.org/hco/12/GRCh38#132200795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110763986-C-A

132200795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110763986-C-T

http://identifiers.org/hco/12/GRCh38#132200815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110763958-C-A

132200815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110763958-C-T

http://identifiers.org/hco/12/GRCh38#132200825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110763948-C-A

132200825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110763948-C-T

132201030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110763486-G-A

132201030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110763486-G-T

132201170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110763352-A-G

http://identifiers.org/hco/12/GRCh38#132201185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110763337-C-A

132201185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 110763337-C-T

132201233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110763289-G-A

132201233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110763289-G-C

132203572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 110762060-C-T

132203599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 110762033-T-A

132203599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 110762033-T-C

132228743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron variant
orthologous variants: 110756852-G-A

132228771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron variant
orthologous variants: 110756878-C-T

132228809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron variant
orthologous variants: 110756913-G-A

132228809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron variant
orthologous variants: 110756913-G-T

132228920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron variant
orthologous variants: 110757026-T-C

132229088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron variant
orthologous variants: 110757191-G-A

132229088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron variant
orthologous variants: 110757191-G-C

132247961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110750511-C-T

http://identifiers.org/hco/12/GRCh38#132248007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110750465-C-A

132248127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110750362-T-A

132248127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110750362-T-C

132248147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110750338-T-A

132248149-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110750336-T-A

132248149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110750336-T-G

132248592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110750131-T-A

http://identifiers.org/hco/12/GRCh38#132248683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110750033-C-A

132248683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110750033-C-T

132248821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110749884-T-C

132249886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110748768-C-G

132249886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110748768-C-T

132249929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110748731-C-T

http://identifiers.org/hco/12/GRCh38#132249969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110748683-C-A

132249979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110748675-T-C

132249988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110748666-G-A

132256766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110746241-T-C

132256779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110746228-C-T

132256982-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110746042-T-G

132257097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110745932-G-A

132257256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110745764-C-T

132257779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110744037-G-A

132257906-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110743908-A-T

http://identifiers.org/hco/12/GRCh38#132257918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110743896-C-A

132257918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110743896-C-T

132258349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110743583-T-C

132258433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110743495-C-T

http://identifiers.org/hco/12/GRCh38#132258455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110743482-C-A

132258455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110743482-C-T

132258530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110743401-G-A

132258530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110743401-G-C

132258766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110743184-G-A

132258842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110743111-C-T

132258844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110743109-G-A

132259152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110742859-C-G

132259152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110742859-C-T

132259208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110742805-T-C

132259208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110742805-T-G

132259338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110742676-A-G

132259371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110742648-G-A

http://identifiers.org/hco/12/GRCh38#132259471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110742558-C-A

132259471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110742558-C-T

132259539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110742491-C-T

132259600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110742389-G-C

132259612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110742375-C-G

132259612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110742375-C-T

132259871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110741754-T-G

132259886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110741739-T-G

132260996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110737759-G-C

132261002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110737753-G-A

http://identifiers.org/hco/12/GRCh38#132261207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110737558-C-A

132261207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110737558-C-T

http://identifiers.org/hco/12/GRCh38#132262458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110736273-C-A

132262458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 110736273-C-T

132263297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110733282-G-T

132273646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110731284-A-G

http://identifiers.org/hco/12/GRCh38#132276517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110728990-C-A

132276665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110728857-T-C

132276851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110728673-G-T

132276870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110728658-A-G

http://identifiers.org/hco/12/GRCh38#132278301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110727487-A-C

http://identifiers.org/hco/12/GRCh38#132278322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110727464-C-A

132285846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110725768-A-G

http://identifiers.org/hco/12/GRCh38#132285951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110725665-C-A

http://identifiers.org/hco/12/GRCh38#132286408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110725326-C-A

http://identifiers.org/hco/12/GRCh38#132286504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#110725239-C-A

132286504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110725239-C-T

132288265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110723535-G-A

http://identifiers.org/hco/12/GRCh38#132294739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110719838-A-C

132294739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110719838-A-T

132294751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110719826-C-G

132294751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110719826-C-T

http://identifiers.org/hco/12/GRCh38#132294755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110719812-C-A

132294755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110719812-C-G

132307002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110713013-A-G

http://identifiers.org/hco/12/GRCh38#132309931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110711320-C-A

132310131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110711126-T-C

132310447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110710845-G-A

132310447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110710845-G-T

132310480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110710832-C-T

132310513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110710798-G-A

132310513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110710798-G-T

132310588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110710722-G-T

132311261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110710148-C-T

http://identifiers.org/hco/12/GRCh38#132311323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110710086-C-A

132311479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110709975-G-A

132311793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110709704-C-T

132311798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110709699-G-A

132311858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110709643-G-A

132311859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110709642-G-T

132312012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110709489-C-T

132312377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110709161-G-A

http://identifiers.org/hco/12/GRCh38#132314065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110708962-C-A

132314065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110708962-C-T

132314656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110708529-G-A

132314656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110708529-G-T

132314763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110708450-T-C

132314938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110708044-G-A

132318401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110703404-C-T

132323545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110697865-G-A

132323662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110697748-C-T

132323789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110697629-T-C

132323873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110697583-G-A

132323931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110697552-C-G

132323931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110697552-C-T

132324056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110697450-T-C

132324071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110697435-C-G

132326339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110695190-G-A

132326339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110695190-G-T

132326440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110695095-A-G

132326544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110695040-C-T

132327312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110694393-T-C

http://identifiers.org/hco/12/GRCh38#132327785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110693981-A-C

132328090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110693760-C-T

132328163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110693687-G-A

132328399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110693459-C-T

132328534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110693322-C-T

132328615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110693228-G-A

132328724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110693034-G-A

132328893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110692876-T-C

http://identifiers.org/hco/12/GRCh38#132328928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110692841-C-A

132328928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110692841-C-T

http://identifiers.org/hco/12/GRCh38#132329033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110692739-C-A

132329052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110692720-T-A

132329242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110692525-C-G

132329242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110692525-C-T

132329278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110692484-G-A

http://identifiers.org/hco/12/GRCh38#132329356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110692419-C-A

132329356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 5 prime UTR variant
orthologous variants: 110692419-C-G

132329356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 5 prime UTR variant
orthologous variants: 110692419-C-T

132329415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 5 prime UTR variant
orthologous variants: 110692361-G-A

132329450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4131
most severe consequence: 5 prime UTR variant
orthologous variants: 110692330-G-T