153991831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 3 prime UTR variant
orthologous variants: 57373890-T-C

http://identifiers.org/hco/5/GRCh38#153991872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57373930-A-C

153991986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 3 prime UTR variant
orthologous variants: 57374018-G-A

153992534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 3 prime UTR variant
orthologous variants: 57374412-G-A

153992534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 3 prime UTR variant
orthologous variants: 57374412-G-C

153992693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57374559-G-T

153992697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57374563-G-A

153992697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57374563-G-C

153992697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57374563-G-T

153992807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57374675-G-A

153992807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57374675-G-T

153992810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57374678-T-C

http://identifiers.org/hco/5/GRCh38#153992861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57374723-C-A

153992861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57374723-C-G

153992861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57374723-C-T

153992884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57374741-A-G

153992893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57374750-A-T

153992957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57374814-G-A

http://identifiers.org/hco/5/GRCh38#153993001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57374858-C-A

153993001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57374858-C-T

153993304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57375161-G-A

153993653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57376866-G-C

http://identifiers.org/hco/5/GRCh38#153993750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57376949-A-C

153993922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57377108-G-A

153993923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57377109-A-G

153993931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57377117-T-C

http://identifiers.org/hco/5/GRCh38#153993940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57377126-C-A

153993996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57377187-G-C

153994345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57377674-T-C

153994385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57377715-G-A

153994385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57377715-G-T

153994438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57377924-A-T

http://identifiers.org/hco/5/GRCh38#153994482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57377970-C-A

153994581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57378058-G-T

153994608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57378083-G-T

153994662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57378137-C-T

153994683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57378158-G-A

153994685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57378160-A-G

153994764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57378243-A-G

153994775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57378254-A-T

153994776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57378255-T-C

http://identifiers.org/hco/5/GRCh38#153994988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57378462-C-A

153995013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57378483-A-G

153995036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57378497-T-C

http://identifiers.org/hco/5/GRCh38#153995053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57378514-C-A

153995053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57378514-C-T

153995080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57378552-T-C

153995080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57378552-T-G

153995097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57378570-G-A

153995097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57378570-G-T

153995210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57378689-T-A

153995210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57378689-T-C

153997672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57380827-G-A

153997672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57380827-G-T

http://identifiers.org/hco/5/GRCh38#153997718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57380870-C-A

153997746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57380889-T-C

153997793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57380926-G-A

153997793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57380926-G-C

153997793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57380926-G-T

153997807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57380940-G-A

153997807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57380940-G-T

153997990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron variant
orthologous variants: 57381126-A-G

153998002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron variant
orthologous variants: 57381136-G-C

153998004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron variant
orthologous variants: 57381138-G-A

153998004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron variant
orthologous variants: 57381138-G-C

153998005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron variant
orthologous variants: 57381139-T-C

153998005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron variant
orthologous variants: 57381139-T-G

153998009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron variant
orthologous variants: 57381143-T-C

http://identifiers.org/hco/5/GRCh38#153998011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57381145-C-A

153998011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron variant
orthologous variants: 57381145-C-G

154001683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron variant
orthologous variants: 57382241-T-C

154001878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron variant
orthologous variants: 57382395-T-C

154002016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron variant
orthologous variants: 57382534-T-C

154002016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron variant
orthologous variants: 57382534-T-G

http://identifiers.org/hco/5/GRCh38#154002112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57382621-C-A

154002112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron variant
orthologous variants: 57382621-C-G

154002112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron variant
orthologous variants: 57382621-C-T

154002446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57382946-C-T

154002680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57383210-T-G

http://identifiers.org/hco/5/GRCh38#154002729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57383253-C-A

154002729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57383253-C-T

154002758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57383276-G-A

154002758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57383276-G-C

154002758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57383276-G-T

154002986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57383966-T-C

154003042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57384000-A-G

http://identifiers.org/hco/5/GRCh38#154003052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57384010-C-A

http://identifiers.org/hco/5/GRCh38#154003105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57384059-C-A

154003105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57384059-C-T

154010502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57389780-T-G

http://identifiers.org/hco/5/GRCh38#154010506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57389784-C-A

154010506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57389784-C-T

154010811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57390030-C-G

154010944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57390120-G-C

http://identifiers.org/hco/5/GRCh38#154011023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57390193-C-A

154011040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57390210-C-T

http://identifiers.org/hco/5/GRCh38#154011124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57390300-C-A

154011124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57390300-C-G

154011124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57390300-C-T

http://identifiers.org/hco/5/GRCh38#154011187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57390498-C-A

154011187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57390498-C-T

http://identifiers.org/hco/5/GRCh38#154011188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57390499-C-A

154011188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57390499-C-G

154011188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57390499-C-T

http://identifiers.org/hco/5/GRCh38#154011270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57390581-C-A

154011270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57390581-C-T

154011333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57390643-G-T

154011339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57390649-T-C

154012470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57391762-T-C

154012520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57391811-T-A

154012556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57391846-C-T

154012679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57391970-T-C

http://identifiers.org/hco/5/GRCh38#154013231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57392500-A-C

154013313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57392576-G-A

154013353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57392599-A-G

http://identifiers.org/hco/5/GRCh38#154013393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57392630-C-A

154013483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57392746-G-A

154013893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57393291-C-T

154013903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57393301-C-T

154014133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57393522-C-G

154025863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57395698-T-C

154026065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57395880-T-C

http://identifiers.org/hco/5/GRCh38#154026207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57395983-C-A

154026262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57396004-A-G

154026339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57396029-A-G

154026339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57396029-A-T

http://identifiers.org/hco/5/GRCh38#154026630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57396270-C-A

154026630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57396270-C-G

154026805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57397112-T-G

154026834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57397141-T-G

154026951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57397497-T-G

154027013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57397552-C-T

154027352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57397839-C-T

154027377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57397864-G-A

154027377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57397864-G-T

154027389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57397876-G-A

154027389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57397876-G-C

154027389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57397876-G-T

154027408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57397895-G-A

154027408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57397895-G-T

http://identifiers.org/hco/5/GRCh38#154027442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57397927-C-A

154027442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57397927-C-T

http://identifiers.org/hco/5/GRCh38#154027482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57397967-C-A

154027482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57397967-C-T

http://identifiers.org/hco/5/GRCh38#154027488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57397973-C-A

154027488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57397973-C-G

154027488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57397973-C-T

154028158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57398328-T-C

154028203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57398373-A-G

http://identifiers.org/hco/5/GRCh38#154028563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57399079-C-A

154029402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57400146-T-C

154029414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57400158-G-A

154029414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57400158-G-T

154029606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57400316-C-G

154029606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57400316-C-T

http://identifiers.org/hco/5/GRCh38#154029654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57400359-A-C

154029686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57400580-A-G

154029701-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57400595-T-A

154029701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57400595-T-C

154029729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57400625-T-C

154029913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57400785-G-A

154030046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57400860-T-C

154030380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57401413-T-C

154030644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57401641-G-A

154030683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57401667-G-A

154030758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57401710-T-C

154031030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57401974-G-A

154031030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57401974-G-C

154033518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57403837-T-C

154033616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57403902-A-G

154033696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57403972-G-A

154033696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57403972-G-T

154033698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57403974-G-A

154033698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57403974-G-C

154033707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57403983-G-T

154033734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57404023-G-T

154033758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57404046-T-A

154033758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57404046-T-C

154033758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57404046-T-G

154033792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 57404069-T-C

154034091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57404398-T-A

154034106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57404412-C-T

http://identifiers.org/hco/5/GRCh38#154034246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57404429-C-A

154034246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57404429-C-T

154034279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 57404463-T-C

http://identifiers.org/hco/5/GRCh38#154034294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57404478-A-C

154034467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57404651-T-C

http://identifiers.org/hco/5/GRCh38#154034488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57404670-C-A

154034664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57404841-T-C

http://identifiers.org/hco/5/GRCh38#154034674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57404851-C-A

154034756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57404933-A-G

154034935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57405082-T-C

154034938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57405085-C-G

154034966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 57405113-A-G

154034966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 57405113-A-T

154034998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57405145-T-C

154035003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57405150-G-A

154035003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57405150-G-T

154035007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57405158-C-T

154035074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57405214-G-A

http://identifiers.org/hco/5/GRCh38#154035091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57405233-C-A

154035112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57405254-C-T

154035244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57405355-G-A

154035244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57405355-G-C

154035927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57406313-C-T

154036032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57406437-T-C

154036095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57406503-A-G

154036129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57406531-T-A

154036354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57406930-T-C

154036473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57407036-G-A

154036499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57407077-T-G

154036592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57407146-A-G

154036626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57407208-T-C

154036739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57407392-T-C

154036913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57407558-C-T

http://identifiers.org/hco/5/GRCh38#154037049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57407686-C-A

http://identifiers.org/hco/5/GRCh38#154037074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57407711-C-A

154037078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57407715-T-C

154037088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57407724-G-A

http://identifiers.org/hco/5/GRCh38#154037105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57407741-C-A

154037105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57407741-C-T

154037300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57408360-G-A

154037306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57408366-A-G

154037507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57408577-T-C

154038172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57408990-A-G

154038338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57409129-G-A

154038432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 57409172-T-C

154038444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57409179-T-C

154038447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57409182-A-G

http://identifiers.org/hco/5/GRCh38#154038591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
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/11/GRCm39#57409212-A-C

154038591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57409212-A-G

154038598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57409219-C-G

154038678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57409283-G-A

154038678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57409283-G-T

154038706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57409312-C-T

154038728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57409322-A-G

154038728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57409322-A-T

http://identifiers.org/hco/5/GRCh38#154038729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
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/11/GRCm39#57409323-C-A

154038729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57409323-C-T

154038730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57409324-A-G

http://identifiers.org/hco/5/GRCh38#154038734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
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/11/GRCm39#57409328-C-A

154038734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57409328-C-T

http://identifiers.org/hco/5/GRCh38#154038856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57409379-C-A

154038856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 57409379-C-T

154038932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1333
most severe consequence: 5 prime UTR variant
orthologous variants: 57409462-C-T