32741878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 5 prime UTR variant
orthologous variants: 129142226-G-A

32741878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 5 prime UTR variant
orthologous variants: 129142226-G-T

http://identifiers.org/hco/1/GRCh38#32741913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129142189-C-A

32741913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 5 prime UTR variant
orthologous variants: 129142189-C-T

32741961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: missense variant
orthologous variants: 129142131-G-A

32741961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: missense variant
orthologous variants: 129142131-G-T

32742012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: missense variant
orthologous variants: 129142080-G-A

32742012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: missense variant
orthologous variants: 129142080-G-C

32742012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: missense variant
orthologous variants: 129142080-G-T

32742150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: missense variant
orthologous variants: 129141951-G-A

32742150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: missense variant
orthologous variants: 129141951-G-T

http://identifiers.org/hco/1/GRCh38#32742168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129141933-A-C

32742168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: missense variant
orthologous variants: 129141933-A-G

32742168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: missense variant
orthologous variants: 129141933-A-T

32742228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129141879-T-C

http://identifiers.org/hco/1/GRCh38#32742229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129141878-C-A

32742229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129141878-C-T

32742243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129141864-A-G

32742243-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129141864-A-T

32742385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129141738-C-T

32742390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129141733-C-T

32742395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129141728-A-T

32742478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129141644-T-G

32742500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129141633-G-C

32742963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129141161-G-T

32743003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129141118-G-A

32743031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129141090-C-T

32743100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129141000-T-C

32743140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129140954-G-C

32743233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129140866-G-A

http://identifiers.org/hco/1/GRCh38#32743451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129140658-C-A

32743451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129140658-C-G

32743644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129140467-G-A

http://identifiers.org/hco/1/GRCh38#32743991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129140149-C-A

32744505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129139524-T-C

32744772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129139322-T-C

32744812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129139288-C-T

32744880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129139200-T-A

32744880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129139200-T-C

32745843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129138933-G-C

32745907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129138870-T-A

32746363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, undefined
orthologous variants: 129138746-G-T

32746407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, undefined
orthologous variants: 129138704-C-T

32746485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129138576-T-C

32746693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129138351-G-A

32747224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129137928-C-T

32747318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129137835-G-A

32747318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129137835-G-T

32748934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129137498-C-T

32749486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129136543-C-T

32749662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129136346-C-T

32749939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129136036-A-G

32750009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129135975-T-C

32750010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129135974-C-T

32750194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129135807-G-A

32750410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129135590-C-G

32750468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129135527-C-G

32752397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129134212-G-T

32753737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129133244-C-G

http://identifiers.org/hco/1/GRCh38#32753981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129132996-C-A

32753981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129132996-C-T

32753983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129132994-C-G

32753983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129132994-C-T

32753986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129132991-G-A

32754026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129132951-G-A

32754026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129132951-G-T

http://identifiers.org/hco/1/GRCh38#32754053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129132924-C-A

32754053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129132924-C-T

http://identifiers.org/hco/1/GRCh38#32754239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129132747-C-A

32754239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129132747-C-G

32754239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129132747-C-T

32754251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129132732-C-T

32754261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129132722-G-T

http://identifiers.org/hco/1/GRCh38#32754353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129132633-C-A

32754570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129132438-C-T

http://identifiers.org/hco/1/GRCh38#32754744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129132289-C-A

32754837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129132202-G-A

32754962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129132093-C-T

32755010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129132038-G-A

32755094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129131948-G-A

32755249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129131789-G-C

32755605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129131421-A-T

32757112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129130419-C-T

32757228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129130341-G-C

32757436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129130122-G-T

32757631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129129979-C-T

32757793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129129842-G-A

http://identifiers.org/hco/1/GRCh38#32757940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129129707-A-C

32758166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129129506-C-T

32758505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129129195-T-C

32758549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129129148-G-A

32758632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129129064-C-T

http://identifiers.org/hco/1/GRCh38#32758814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129128604-A-C

32758835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129128595-C-G

32759042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129128422-G-A

32759184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129127128-T-A

32759578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129126740-C-T

32759620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129126688-G-T

32760409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129125958-C-G

32760996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129125692-G-A

32760997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129125691-C-T

32761113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129125548-G-A

32761131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129125530-C-T

32761218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129125448-C-T

32761313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129125358-G-A

32761548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129125137-T-G

32761645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129125051-A-G

32761833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129124922-C-T

32761940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129124817-C-T

32761953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129124804-A-G

32762059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129124698-A-G

32764943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129122354-C-G

32765098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129122243-A-G

32765150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129122188-T-C

32765194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129122145-C-G

32765235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129122120-G-T

32765292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129122066-G-A

32765501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129121824-G-A

32765501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129121824-G-T

32765516-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129121811-T-A

32765564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129121764-G-A

http://identifiers.org/hco/1/GRCh38#32765791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129121551-C-A

32765791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 129121551-C-T

http://identifiers.org/hco/1/GRCh38#32765908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129121443-A-C

32765908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129121443-A-G

32765908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129121443-A-T

32765933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129121419-G-T

32765973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129121378-T-C

32766093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129121259-T-A

32766093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129121259-T-G

32766150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129121202-T-A

32766539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129120883-G-T

32767007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129120427-C-T

32767477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129120042-C-T

32767479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129120040-G-A

32767539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129120001-C-T

32767687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129119888-T-C

32767710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129119878-G-A

32767710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129119878-G-T

http://identifiers.org/hco/1/GRCh38#32767726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129119862-C-A

http://identifiers.org/hco/1/GRCh38#32767819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129119772-A-C

32768643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129119272-C-T

32768664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129119251-G-A

32768724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129119194-T-C

32768727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129119191-A-G

http://identifiers.org/hco/1/GRCh38#32768751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129119167-C-A

32768751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129119167-C-G

32768751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129119167-C-T

http://identifiers.org/hco/1/GRCh38#32768893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129119006-C-A

32768977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129118926-G-A

32768977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129118926-G-T

32769376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129118556-A-G

32769488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129118442-A-G

32769515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129118405-C-T

http://identifiers.org/hco/1/GRCh38#32769525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129118395-C-A

32769525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129118395-C-G

32769525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129118395-C-T

32769650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129118328-T-C

http://identifiers.org/hco/1/GRCh38#32769656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129118322-C-A

32769656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129118322-C-G

32769820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129118159-G-T

http://identifiers.org/hco/1/GRCh38#32770009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129117978-C-A

32770009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: 129117978-C-T

32770191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: 129117796-C-G

32770191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 129117796-C-T

http://identifiers.org/hco/1/GRCh38#32770245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129117742-C-A

32770350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: 129117637-C-G

32770350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: 129117637-C-T

32770505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 129117482-G-A

32770527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: 129117460-A-G

http://identifiers.org/hco/1/GRCh38#32770537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129117450-C-A

32770651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: 129117336-T-C

32770775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 129117212-G-A

32770775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: 129117212-G-T

http://identifiers.org/hco/1/GRCh38#32770782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129117205-C-A

32770782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: 129117205-C-T

32771118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: 129116869-G-A

http://identifiers.org/hco/1/GRCh38#32771171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129116816-C-A

32771171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 129116816-C-G

32771171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 129116816-C-T

32771272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: 129116715-C-G

32771315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 129116672-A-G

32771418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: 129116569-C-T

http://identifiers.org/hco/1/GRCh38#32771487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129116500-C-A

32771487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: 129116500-C-T

32771628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: 129116374-G-A

32771628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: 129116374-G-C

32771699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 129116333-A-G

http://identifiers.org/hco/1/GRCh38#32771773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129116268-A-C

32771773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: 129116268-A-T

32771799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: 129116242-G-A

32771799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: 129116242-G-T

32771803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: 129116238-G-A

32771803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: 129116238-G-T

http://identifiers.org/hco/1/GRCh38#32771874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129116167-C-A

32771874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: 129116167-C-T

32771931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: 129116110-G-A

32771931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: 129116110-G-C

http://identifiers.org/hco/1/GRCh38#32771934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129116107-C-A

32771934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: 129116107-C-T

32772243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: 129115795-C-G

32772243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: 129115795-C-T

http://identifiers.org/hco/1/GRCh38#32772278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129115760-C-A

32772278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 129115760-C-G

32772278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 129115760-C-T

http://identifiers.org/hco/1/GRCh38#32772308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129115733-A-C

32772308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 129115733-A-G

32772308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 129115733-A-T

32772409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: 129115635-G-A

32772409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, missense_variant
orthologous variants: 129115635-G-T

32772507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129115564-G-A

32772507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129115564-G-T

32772513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129115558-G-A

32772513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129115558-G-T

http://identifiers.org/hco/1/GRCh38#32772556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129115514-C-A

32772556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129115514-C-G

32772556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129115514-C-T

http://identifiers.org/hco/1/GRCh38#32772575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129115495-C-A

32772585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129115481-G-T

32772593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129115473-G-A

32772593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129115473-G-T

32772785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129115336-G-A

32772785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129115336-G-C

32772829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron variant
orthologous variants: 129115298-G-A

http://identifiers.org/hco/1/GRCh38#32772858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#129115275-C-A

32772858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 129115275-C-G

32772858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 129115275-C-T

http://identifiers.org/hco/1/GRCh38#32772978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129115154-C-A

32772978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: 129115154-C-T

32773098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 129115038-T-C

32773107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 129115029-G-A

32773107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 129115029-G-T

32773171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 129114969-G-A

32773171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 129114969-G-C

32773171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 129114969-G-T

http://identifiers.org/hco/1/GRCh38#32773184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#129114956-C-A

32773184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 129114956-C-T

http://identifiers.org/hco/1/GRCh38#32773223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#129114916-C-A

32773223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 129114916-C-T

http://identifiers.org/hco/1/GRCh38#32773247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129114895-C-A

32773247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: 129114895-C-T

32773389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: 129114756-T-C

http://identifiers.org/hco/1/GRCh38#32773415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129114732-C-A

32773415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: 129114732-C-T

32773440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: 129114704-C-G

32773440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: 129114704-C-T

http://identifiers.org/hco/1/GRCh38#32773444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129114700-A-C

32773444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: 129114700-A-G

http://identifiers.org/hco/1/GRCh38#32773603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129114540-C-A

32773603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: 129114540-C-T

32773713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: 129114406-G-T

32773770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: 129114335-G-T

32773778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: 129114327-G-A

32773778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: 129114327-G-T

http://identifiers.org/hco/1/GRCh38#32773828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129114287-A-C

32773828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: 129114287-A-G

http://identifiers.org/hco/1/GRCh38#32773898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129114223-C-A

32773898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: 129114223-C-T

32774006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: 129114122-C-G

32774006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: 129114122-C-T

http://identifiers.org/hco/1/GRCh38#32774094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129114051-C-A

http://identifiers.org/hco/1/GRCh38#32774120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129114027-C-A

32774120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: 129114027-C-T

http://identifiers.org/hco/1/GRCh38#32774161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129114003-C-A

32774161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: 129114003-C-T

http://identifiers.org/hco/1/GRCh38#32774206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129113965-C-A

32774206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: 129113965-C-T

32774285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 129113897-G-A

32774285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 129113897-G-C

32774285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 129113897-G-T

http://identifiers.org/hco/1/GRCh38#32774288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#129113894-C-A

32774315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: 129113861-A-G

http://identifiers.org/hco/1/GRCh38#32774415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129113793-C-A

32774589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 129113701-G-A

http://identifiers.org/hco/1/GRCh38#32774590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#129113700-C-A

32774590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 129113700-C-G

32774590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 129113700-C-T

32774663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29301
most severe consequence: 3 prime UTR variant
orthologous variants: 129113677-G-T