158124566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79852620-T-G

158124679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79852508-G-T

158124689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79852291-A-G

158124849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79851982-A-G

158125019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79851841-T-C

158125158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79851709-T-C

158125159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79851708-T-A

158125159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79851708-T-C

http://identifiers.org/hco/4/GRCh38#158125315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79851331-C-A

158125323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79851323-T-C

158125747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79850980-A-G

158125866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79850851-T-C

158125972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79850749-G-T

http://identifiers.org/hco/4/GRCh38#158125980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79850741-C-A

158126038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79850693-A-G

158126042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79850690-T-C

158126261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79850332-A-T

http://identifiers.org/hco/4/GRCh38#158126262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79850331-A-C

158126262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79850331-A-G

158126450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79850149-A-T

158126463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79850136-G-A

158126463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79850136-G-T

158126529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79850080-T-A

158126529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79850080-T-C

http://identifiers.org/hco/4/GRCh38#158127077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79849141-C-A

158127077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79849141-C-T

158127083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79849135-T-A

158127105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79849114-G-A

158127168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79849051-T-C

158127168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79849051-T-G

158127178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79849041-T-C

158127193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79849026-A-G

158127290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79848918-T-C

158127291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3 prime UTR variant
orthologous variants: 79848917-A-T

http://identifiers.org/hco/4/GRCh38#158127459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79848755-A-C

158127619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 79848595-A-G

http://identifiers.org/hco/4/GRCh38#158127637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79848577-C-A

158127646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79848568-T-C

http://identifiers.org/hco/4/GRCh38#158127665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79848546-C-A

http://identifiers.org/hco/4/GRCh38#158127674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79848539-C-A

158127677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79848536-C-T

158127689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79848524-T-C

158128079-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79848164-T-G

158128192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79848056-T-C

158128302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79846908-G-T

158128410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79846784-T-C

158128686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79846557-G-T

158128730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79846531-C-T

158128739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79846523-G-C

http://identifiers.org/hco/4/GRCh38#158128751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79846511-C-A

158128751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79846511-C-T

158128752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79846510-G-A

158128786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79846481-C-T

158128838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79846428-T-C

158128986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79846301-T-C

158129188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79846094-G-T

http://identifiers.org/hco/4/GRCh38#158129390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79845900-C-A

158129390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79845900-C-G

http://identifiers.org/hco/4/GRCh38#158129454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79845841-C-A

158129654-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79845642-T-A

158129911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79845433-C-T

158129942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79845402-G-A

158130109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79844961-T-C

158130167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79844906-A-G

158130205-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79844868-T-G

158130383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79844681-T-C

158130419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79844644-T-C

158130444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79844618-C-T

158130500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79844578-A-G

158130535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79844544-G-A

158130580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79844499-T-C

158130690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron variant
orthologous variants: 79844411-G-T

158130903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79844009-A-G

158130903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79844009-A-T

158130914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79843998-A-G

158131090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79843819-G-A

158131167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79843742-C-G

158131254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79843664-G-T

158131260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79843658-C-T

http://identifiers.org/hco/4/GRCh38#158131330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79843590-C-A

158131330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79843590-C-T

158131444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79843478-T-C

158133649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79842104-A-G

158133649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79842104-A-T

158133777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79841978-C-T

http://identifiers.org/hco/4/GRCh38#158133821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79841939-A-C

158133886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79841873-G-C

158133907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79841852-G-C

158134089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79841698-C-T

http://identifiers.org/hco/4/GRCh38#158134171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79841624-C-A

158134252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79841539-A-T

158134302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79841490-A-G

158134917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79840656-G-A

http://identifiers.org/hco/4/GRCh38#158135560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79840506-C-A

158135560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79840506-C-T

http://identifiers.org/hco/4/GRCh38#158135579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79840486-C-A

158135579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79840486-C-T

158135690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79840371-G-A

158135703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79840361-G-T

158135787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79840269-C-T

158135798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79840256-A-G

http://identifiers.org/hco/4/GRCh38#158136046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79840179-A-C

158136049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79840176-T-C

158136067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79840158-T-C

http://identifiers.org/hco/4/GRCh38#158137426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79838423-C-A

158137721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79838022-C-T

http://identifiers.org/hco/4/GRCh38#158137722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79838021-C-A

158137722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79838021-C-G

158137722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79838021-C-T

http://identifiers.org/hco/4/GRCh38#158137886-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79837877-A-C

http://identifiers.org/hco/4/GRCh38#158137940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79837825-C-A

158138000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79837776-T-A

158138087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79837688-G-A

158138195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79837640-T-C

158138650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79836872-T-C

158138943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79836585-T-C

158139165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79836382-C-T

158139167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79836380-T-C

158139174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79836373-C-T

158139196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79836353-A-G

158139287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79836257-T-C

158139886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79836100-C-T

158140003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79835985-G-A

158140005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79835983-G-A

http://identifiers.org/hco/4/GRCh38#158140072-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79835925-A-C

158140073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79835924-C-T

http://identifiers.org/hco/4/GRCh38#158140111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79835890-A-C

158140111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79835890-A-G

158140122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79835879-G-A

158140178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79835828-A-G

158140241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79835768-C-G

158140241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79835768-C-T

158140295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79835713-A-G

158140384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79835617-C-T

158140510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79835463-G-C

158140604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79835376-G-A

158140740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79835277-C-T

http://identifiers.org/hco/4/GRCh38#158141166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79834902-A-C

158143134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79831756-A-G

158143190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79831699-T-C

158143192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79831697-G-T

158143272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79831629-T-C

158143537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79831271-G-C

158143549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79831259-T-C

158143816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79830996-A-G

158143830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79830985-C-T

http://identifiers.org/hco/4/GRCh38#158143862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79830964-C-A

158144278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79830427-A-G

158144462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79830304-T-A

158144723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79829244-G-A

158144824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79829144-T-C

158144878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79829094-G-A

158144901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79829071-A-G

158145041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79828930-G-A

http://identifiers.org/hco/4/GRCh38#158145768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79828010-C-A

http://identifiers.org/hco/4/GRCh38#158145892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79827898-C-A

158146009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79827805-T-C

158146148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79827671-T-C

158146148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79827671-T-G

http://identifiers.org/hco/4/GRCh38#158146537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79827280-C-A

158146537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79827280-C-G

158146555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79827263-G-A

158146559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79827259-C-G

158146833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79827017-C-T

158146953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79826898-T-C

158146963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79826887-T-C

158147053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79826801-A-G

http://identifiers.org/hco/4/GRCh38#158147135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79826721-C-A

158147278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79826595-A-G

158147715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79826504-C-T

http://identifiers.org/hco/4/GRCh38#158147760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79826468-C-A

158148868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79817987-A-G

158148898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79817959-G-A

158149008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79817856-T-A

158149027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79817837-G-A

158149059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79817806-G-A

158149095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79817772-T-C

158149130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79817739-C-G

158149130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79817739-C-T

158149276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79817574-T-C

158149431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79817401-G-A

158149503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79817325-A-G

158149546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79817283-A-G

158150290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79817046-T-C

158150734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79816626-A-T

158150735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79816625-T-C

158150775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79816587-T-A

158150775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79816587-T-C

158150802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79816562-C-T

158150865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79816499-T-C

158155514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79816191-T-A

158155528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79816177-A-G

158155574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79816143-G-T

158155867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79815847-G-A

158155928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79815789-A-G

158155928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79815789-A-T

158155931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79815786-G-A

158155931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79815786-G-T

158155937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79815780-G-T

158155942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79815776-A-G

http://identifiers.org/hco/4/GRCh38#158155948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79815770-C-A

158155948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79815770-C-T

158156389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79815316-A-T

158156544-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79815160-T-G

158156658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79815054-T-A

158156677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79815035-A-G

158156722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79814992-T-C

158156743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79814971-A-G

158156747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79814967-C-G

158156747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79814967-C-T

158156844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79814867-G-A

158156908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79814805-A-T

http://identifiers.org/hco/4/GRCh38#158157211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79814576-C-A

158157379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79814418-G-A

158157435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79814362-T-A

158157435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79814362-T-C

158157654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79814152-G-T

158157681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79814125-A-T

158157714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79814090-C-T

158157751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79814057-T-C

158157777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79814035-T-C

158158098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79813698-T-C

http://identifiers.org/hco/4/GRCh38#158158265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79813310-C-A

158158266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79813309-A-G

http://identifiers.org/hco/4/GRCh38#158158338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79813236-C-A

158158359-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79813215-T-A

158158366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79813208-G-A

158158386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79813188-A-G

158158638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79812941-C-G

http://identifiers.org/hco/4/GRCh38#158158743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79812845-A-C

158158837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79812749-T-A

158158857-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79812728-A-T

158159269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79812064-A-T

158159399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79811935-G-A

158159501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79811833-G-A

158159501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79811833-G-C

158159580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79811754-G-A

158159756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79811577-G-A

158159756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79811577-G-C

158159756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79811577-G-T

158159844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79811487-G-A

158160058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79811279-A-G

158160224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79811111-G-A

158160548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79809331-C-T

158160689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79809196-T-C

158160698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79809187-C-T

158160893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79809054-T-C

158161441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79808242-A-T

158161553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79808118-T-A

158161566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79808102-T-C

158161566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79808102-T-G

158161665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79807970-A-G

158161762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79807846-C-T

158161897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79807732-C-G

158161897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79807732-C-T

158162421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79807323-T-C

158162653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79807102-C-T

http://identifiers.org/hco/4/GRCh38#158162701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79807053-C-A

158162701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79807053-C-T

158162766-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79806989-T-A

158162766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79806989-T-G

158163131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79806611-T-C

158163209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79806546-T-A

158163209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79806546-T-G

158163691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79806370-C-T

158163799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79806296-T-C

158163837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79806258-A-T

http://identifiers.org/hco/4/GRCh38#158163908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79806169-A-C

158164083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79805989-A-G

158164085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79805987-C-G

158164085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79805987-C-T

158164166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79805921-A-G

158164217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79805870-T-C

158164589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79805502-C-T

158164628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79805464-G-A

158164669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79805423-A-G

158164769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79805332-C-T

158164789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79805313-T-A

158164944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79805156-A-T

158165004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79805096-A-G

158165202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79804901-C-T

158165253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79804754-G-A

158165265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79804742-T-A

158165445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79804350-A-G

158165788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79804003-G-T

158165814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79803977-C-T

158165816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79803975-T-C

158165842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79803949-T-C

158166718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79799735-C-T

158166886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79799589-C-T

158166995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79796983-T-G

158167073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79796897-T-C

http://identifiers.org/hco/4/GRCh38#158167089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79796881-C-A

158167089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79796881-C-T

158167099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79796871-G-C

158167099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79796871-G-T

158167173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79796796-T-C

158167466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79796518-A-T

http://identifiers.org/hco/4/GRCh38#158167657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79796329-A-C

158167751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79796270-T-C

158167862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79796196-A-G

158167862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79796196-A-T

158168050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79796052-T-A

158168166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79795936-T-C

158168171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79795934-A-G

158168334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79795787-A-T

158168354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79795767-T-C

158168400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79795713-C-T

158168470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79795645-T-C

158168570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79795558-C-T

158168571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79795557-A-G

158169674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79795456-T-C

158169727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79795403-G-A

158169727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79795403-G-T

158169740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79795390-C-T

158169750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79795380-T-C

158169829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79795311-T-C

158169848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79795298-G-T

http://identifiers.org/hco/4/GRCh38#158169876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79795275-C-A

158169901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79795250-A-G

http://identifiers.org/hco/4/GRCh38#158169968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79795191-A-C

158169968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79795191-A-G

158169968-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79795191-A-T

http://identifiers.org/hco/4/GRCh38#158170019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79795134-C-A

158170019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79795134-C-G

158170019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79795134-C-T

158170125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79794761-G-T

158170192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79794703-A-G

158170216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79794679-G-A

158170238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79794659-T-C

158170254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 79794643-T-G

http://identifiers.org/hco/4/GRCh38#158170263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79794634-C-A

158170263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 79794634-C-T

158170319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 79794580-G-T

158170553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 79794348-T-G

http://identifiers.org/hco/4/GRCh38#158170818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#79794086-C-A

158170818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 79794086-C-G

158170818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 79794086-C-T

158171128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79793779-T-C

158171152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79793755-T-C

158171155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79793752-C-T

158171158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79793749-C-T

http://identifiers.org/hco/4/GRCh38#158171323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79793584-A-C

158171323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79793584-A-G

158171465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79793442-G-A

158171465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79793442-G-C

158171465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79793442-G-T

158171467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79793440-G-A

158171467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79793440-G-C

158171467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79793440-G-T

158171560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79793335-T-C

158171560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79793335-T-G

158171905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79793000-G-A

158172098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79792835-T-C

http://identifiers.org/hco/4/GRCh38#158172115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79792822-A-C

158172173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79792759-T-C

158172175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79792757-T-A

158172175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79792757-T-C

158172179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79792753-T-C

158172181-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79792751-T-A

158172181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79792751-T-C

158172183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79792749-T-A

158172183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79792749-T-C

158172185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79792747-A-T

http://identifiers.org/hco/4/GRCh38#158172338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#79792532-C-A

158172338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79792532-C-T

158172414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79792456-C-T

158172506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79792369-C-T

158172533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79792339-G-A

158172533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79792339-G-C

158172622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79792248-G-T

158172746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79792124-T-C

158172752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79792117-G-A

158172752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79792117-G-T

158172758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79792111-G-A

158172758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79792111-G-T

158172771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79792098-A-G

158172793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79792075-G-T

158172991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79791861-G-T

158172993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79791859-G-A

158172995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79791854-A-G

http://identifiers.org/hco/4/GRCh38#158172996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79791853-C-A

158172999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79791850-A-G

158173148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79791704-G-A

158173148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79791704-G-T

http://identifiers.org/hco/4/GRCh38#158173175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#79791661-C-A

158173175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79791661-C-T

158173251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79791588-G-T

158173305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25312
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79791532-C-T