157785833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3 prime UTR variant
orthologous variants: 45801900-G-T

157786093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3 prime UTR variant
orthologous variants: 45801640-G-T

157786809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45800922-T-A

157786809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45800922-T-C

157786882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45800850-C-T

157786935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45800785-C-T

157787332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45800397-A-G

http://identifiers.org/hco/5/GRCh38#157787408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45800319-C-A

157787414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45800313-G-A

157787414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45800313-G-C

157787414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45800313-G-T

157787445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45800283-C-T

http://identifiers.org/hco/5/GRCh38#157787532-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45800219-A-C

157787532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45800219-A-G

157787567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45800186-T-C

157788136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45799698-T-C

http://identifiers.org/hco/5/GRCh38#157789141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45799086-A-C

157789216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45799024-T-G

http://identifiers.org/hco/5/GRCh38#157789261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45798977-C-A

157789261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45798977-C-G

157789279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45798949-T-G

157789347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45798885-T-C

157789353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45798879-G-C

157789380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45798852-G-A

http://identifiers.org/hco/5/GRCh38#157789727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45798525-C-A

157789736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45798518-T-C

http://identifiers.org/hco/5/GRCh38#157789743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45798511-C-A

157789761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45798486-A-G

157789779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45798476-A-G

157789844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45798425-A-T

157789857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45798412-G-A

157789857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45798412-G-T

http://identifiers.org/hco/5/GRCh38#157789909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45798369-A-C

157790180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45798294-G-A

157790180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45798294-G-T

157790189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45798285-A-G

157790312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45798207-T-C

157790439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 45798090-A-G

http://identifiers.org/hco/5/GRCh38#157790527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45798009-C-A

157790527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45798009-C-G

157790527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45798009-C-T

157790643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45797936-G-A

157790643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45797936-G-C

157791883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45797112-C-T

157791887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45797108-G-A

157791887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45797108-G-T

157792120-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45796876-T-A

http://identifiers.org/hco/5/GRCh38#157792132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45796864-C-A

157792132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45796864-C-T

157792980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45794512-G-T

157793082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45794420-T-C

157793490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45794074-T-C

157793497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45794068-G-A

157794446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45793457-C-T

http://identifiers.org/hco/5/GRCh38#157794951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45793057-C-A

157794951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45793057-C-T

157795096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45792898-T-G

157796954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45790944-C-G

157797015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45790882-T-A

157797736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45790519-T-C

157797823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45790456-T-C

157797885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45790394-G-A

157798338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45790111-G-A

157798367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45790082-T-C

157798400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45790049-G-A

157798405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45790040-C-T

157798753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45789756-T-G

157799273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45789222-A-G

157799273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45789222-A-T

157801117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45787786-C-T

157801118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45787785-G-A

157801870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45787594-T-C

157801870-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45787594-T-G

157803141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45786853-A-G

157803307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45786718-G-A

157803308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45786717-G-C

157803469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45786537-G-A

http://identifiers.org/hco/5/GRCh38#157803713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45785891-C-A

157803713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45785891-C-G

157803713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45785891-C-T

157803767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45785854-A-G

157803815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45785814-T-A

157803815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45785814-T-C

http://identifiers.org/hco/5/GRCh38#157803910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45785729-C-A

http://identifiers.org/hco/5/GRCh38#157805795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45785012-A-C

157805835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45784973-T-G

157805882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45784926-G-C

http://identifiers.org/hco/5/GRCh38#157806077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45784731-C-A

http://identifiers.org/hco/5/GRCh38#157806173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45784633-C-A

157806173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45784633-C-T

157806245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45784568-A-G

http://identifiers.org/hco/5/GRCh38#157806246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45784567-A-C

157806277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45784537-A-G

157806450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45784375-A-T

157806536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45784154-C-T

157806712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45783834-A-T

157807006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45783552-G-C

157808731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45782402-T-C

157809021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45782128-G-T

157809477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45781751-T-A

157809487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45781741-T-A

157809487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45781741-T-C

157809487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45781741-T-G

157809497-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45781731-T-A

157809497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45781731-T-G

http://identifiers.org/hco/5/GRCh38#157809566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45781679-A-C

157809582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45781663-T-C

157810187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45781139-C-T

157810279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45780605-A-G

157810598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45780331-T-C

157812289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45779251-G-A

157812615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45778774-G-A

157812676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45778731-C-T

157812732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45778702-G-A

157812732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45778702-G-C

157813034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45778407-T-G

157813128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: missense variant
orthologous variants: 45778310-T-C

http://identifiers.org/hco/5/GRCh38#157813306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45778138-C-A

http://identifiers.org/hco/5/GRCh38#157813317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45778127-C-A

157813317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45778127-C-G

157813317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45778127-C-T

157813458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45778055-G-A

157813593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45777939-A-G

157813653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45777874-T-A

157813725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45777807-G-A

157813963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45777586-C-G

157814060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45777489-G-A

157814060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45777489-G-T

157814429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45777119-C-G

157814443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45777108-T-A

http://identifiers.org/hco/5/GRCh38#157816225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45775707-A-C

157816277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45775664-T-A

157816277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45775664-T-C

157816422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45775497-A-G

http://identifiers.org/hco/5/GRCh38#157816619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45775320-C-A

157816619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45775320-C-T

157816844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45775143-C-G

157816942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45775044-T-A

157817524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: missense variant
orthologous variants: 45774558-G-A

157817524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: stop gained
orthologous variants: 45774558-G-T

http://identifiers.org/hco/5/GRCh38#157817572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45774498-C-A

157817572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45774498-C-T

http://identifiers.org/hco/5/GRCh38#157817574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45774488-C-A

157817574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45774488-C-T

http://identifiers.org/hco/5/GRCh38#157817855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45774253-C-A

157817900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45774208-G-C

http://identifiers.org/hco/5/GRCh38#157817965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45774150-A-C

157818383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45773779-A-G

157818454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45773759-G-A

157818462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45773751-G-A

157818893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45773610-C-G

157819039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45773479-T-C

157819711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45772878-A-G

157820453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45772466-T-A

http://identifiers.org/hco/5/GRCh38#157822949-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45771876-A-C

157823246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45771681-T-C

157823312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45771614-T-C

157823419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45771519-G-A

157823460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45771476-A-G

157823488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45771450-T-C

157826989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45768646-T-C

157827684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45768350-G-C

157831083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45764119-T-C

157831166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45764042-G-A

157831182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45764028-G-C

157831182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45764028-G-T

157831629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45763858-T-C

157831718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45763769-A-T

157832648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45763609-T-C

157832648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45763609-T-G

157832822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45763473-G-A

157833467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45763192-G-A

157833621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45763051-G-A

157833621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45763051-G-T

157834914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45761986-T-A

157834914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45761986-T-C

157835069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45761847-G-A

157835537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45761446-T-C

157835990-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45761011-T-A

157835990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45761011-T-C

157838491-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45757666-T-A

157838491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45757666-T-C

157842968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45755888-A-G

157843118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45755737-T-C

157843834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45754880-C-T

157844077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45754573-A-G

157844503-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45754038-T-A

157844790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45753776-C-T

157844956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45753614-C-T

157852441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45749021-A-G

157852675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45748792-C-T

157852696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45748771-G-A

157853004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45748525-G-T

157853405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45747607-C-T

http://identifiers.org/hco/5/GRCh38#157855299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45746611-A-C

157855334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45746572-A-G

157855488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45746433-A-G

157856210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45745186-T-C

http://identifiers.org/hco/5/GRCh38#157856607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45744835-C-A

157856607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45744835-C-T

157857416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45744296-A-G

157857573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45744150-G-A

157857618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45744103-A-G

157857639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45744089-T-C

157858012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, undefined
orthologous variants: 45743786-G-A

157858175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45743663-A-G

157858303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45743551-C-T

157858510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45743349-A-G

157858752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45743177-T-C

http://identifiers.org/hco/5/GRCh38#157858863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#45743080-C-A

157858863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45743080-C-G

157858863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron variant
orthologous variants: 45743080-C-T

157858905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, undefined
orthologous variants: 45743042-G-A

157858905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, undefined
orthologous variants: 45743042-G-C

157858905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: intron_variant, undefined
orthologous variants: 45743042-G-T

http://identifiers.org/hco/5/GRCh38#157859045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#45742902-C-A

157859045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 45742902-C-G

157859045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23186
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 45742902-C-T