http://identifiers.org/hco/9/GRCh38#2720513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27303177-C-A

2720514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 27303178-A-G

2720535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 27303199-A-G

2720663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27303319-A-G

http://identifiers.org/hco/9/GRCh38#2720685-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27303341-A-C

2720685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27303341-A-T

2720789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27303439-A-G

2721012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27303644-C-G

2721012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27303644-C-T

2721017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27303649-T-C

2721280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27303919-G-C

2721280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27303919-G-T

2721324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27303964-T-G

2721337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27303976-C-T

2721397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27304034-C-T

2721451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27304085-A-G

2721557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27304190-A-G

2721631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27304245-T-C

2721661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27304275-A-G

2721749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27304353-T-C

2721807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27304411-T-A

2721807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27304411-T-C

2721849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27304454-G-A

2721899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27304503-T-C

http://identifiers.org/hco/9/GRCh38#2722677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27304710-C-A

2722677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27304710-C-G

2722694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27304727-G-T

2722925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 27305135-T-C

http://identifiers.org/hco/9/GRCh38#2723048-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27305279-A-C

2723108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27305338-A-G

http://identifiers.org/hco/9/GRCh38#2723370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27305755-A-C

2723370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27305755-A-G

2723411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27305793-G-C

2723861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27306254-C-T

2723877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27306271-G-A

http://identifiers.org/hco/9/GRCh38#2724151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27306422-C-A

2724151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27306422-C-T

2724260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27306522-T-C

2724372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27306624-G-C

2724372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27306624-G-T

2724690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27306889-G-A

2724972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27307136-C-T

2725007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27307168-T-G

2725096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27307254-T-C

2725127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27307285-G-C

http://identifiers.org/hco/9/GRCh38#2725218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27307378-C-A

2725218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27307378-C-G

2725293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27307442-T-C

2725551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27307612-G-A

2725857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27307899-G-C

2725883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27307918-A-G

2726138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27308144-G-A

http://identifiers.org/hco/9/GRCh38#2726253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27308389-A-C

2726591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27308835-G-A

2726601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27308847-T-G

2726614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27308860-C-G

2726614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27308860-C-T

http://identifiers.org/hco/9/GRCh38#2726644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27308890-C-A

2727069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27308962-T-G

2727177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27309066-C-G

2727448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27309126-C-T

2727452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27309130-C-G

http://identifiers.org/hco/9/GRCh38#2727476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27309154-C-A

2727674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27309365-G-A

2727757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27309431-G-A

2727808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27309496-C-G

2727808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27309496-C-T

2727922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27309615-C-G

2728017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27309706-G-A

2728273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27309940-A-G

2728332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27309995-C-T

http://identifiers.org/hco/9/GRCh38#2728348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#27310010-A-C

2728649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27310302-G-A

2728649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27310302-G-C

http://identifiers.org/hco/9/GRCh38#2728741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27310388-C-A

2729018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27310598-A-G

http://identifiers.org/hco/9/GRCh38#2729046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27310628-C-A

2729046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27310628-C-T

http://identifiers.org/hco/9/GRCh38#2729216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27310844-A-C

2729320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27310929-C-T

http://identifiers.org/hco/9/GRCh38#2729352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27310961-C-A

2729352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27310961-C-G

2729372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27310985-G-T

2729418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27311020-A-G

2729422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27311024-C-T

http://identifiers.org/hco/9/GRCh38#2729790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27311384-A-C

2729807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 27311408-G-A

2729823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 27311424-A-G

2729883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 27311482-G-A

2729883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 27311482-G-C

2729912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 27311510-T-A

2730047-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27311632-A-T

http://identifiers.org/hco/9/GRCh38#2730050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27311635-A-C

2730105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27311691-G-A

2730105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27311691-G-T

2730174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27311762-G-A

2730174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27311762-G-T

2730840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27311958-C-G

2730860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27311978-G-A

2730943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27312069-G-A

2730945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27312071-A-G

2731308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27312357-G-A

2731421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27312476-T-G

2731437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27312492-A-G

2731463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27312519-G-C

2731463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27312519-G-T

2731547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27312635-A-G

http://identifiers.org/hco/9/GRCh38#2732183-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27313389-A-C

2732209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27313414-C-T

http://identifiers.org/hco/9/GRCh38#2732235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27313441-A-C

http://identifiers.org/hco/9/GRCh38#2732256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27313463-C-A

2732798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27313968-C-G

2733210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27314369-G-A

2735379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27316201-T-A

http://identifiers.org/hco/9/GRCh38#2735384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27316206-C-A

2735385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27316207-T-A

2735385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27316207-T-C

2735545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27316349-G-A

2735545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27316349-G-T

2735639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27316436-A-T

2735640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27316437-G-C

2735693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27316474-G-A

2735733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27316501-G-C

2735992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27316717-T-C

2737261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27318904-T-C

http://identifiers.org/hco/9/GRCh38#2737278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27318912-C-A

2737602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27319181-G-A

2737616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27319194-G-T

2737818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27319392-T-G

2737947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27319516-G-A

2738052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27319623-A-G

2738152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27319778-C-T

2738415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27320276-G-A

2738415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27320276-G-C

2738728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27320451-G-A

2738728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27320451-G-C

2738747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27320468-A-G

2738813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27320520-T-A

2738813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27320520-T-C

2738817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27320524-G-A

2738881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27320582-A-G

2738932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27320631-C-T

2739182-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27320851-A-T

2739194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27320868-G-A

2739194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27320868-G-C

2739206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27320880-C-T

2740706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27322420-T-C

2741116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27322757-G-C

2741177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27322803-T-A

2741442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27323078-C-T

2741606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27323348-G-A

http://identifiers.org/hco/9/GRCh38#2741644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27323385-C-A

2741644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27323385-C-T

2741799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27323536-A-T

2745313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27323847-G-A

2745315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27323849-G-C

2745331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27323866-G-C

2745410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27323931-T-C

2745428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27323949-T-A

2745471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27323996-T-C

2745609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27324123-G-A

2745612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27324126-C-G

2745612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27324126-C-T

2745701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27324192-C-G

2745734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27324226-T-C

2745768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27324258-G-T

http://identifiers.org/hco/9/GRCh38#2745891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27324382-A-C

2746165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27324628-C-T

2746172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27324635-G-A

2746172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27324635-G-C

2746283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27324738-A-G

2746291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27324761-T-C

2746309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27324779-C-T

http://identifiers.org/hco/9/GRCh38#2746409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27324870-C-A

2746409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27324870-C-T

2746443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27324904-G-A

2746507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27324989-C-G

http://identifiers.org/hco/9/GRCh38#2746517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27324999-A-C

2746583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27325048-G-A

2746583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27325048-G-C

2747327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27325685-C-T

2747394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27325759-G-C

http://identifiers.org/hco/9/GRCh38#2747572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27325934-A-C

2747610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27325957-A-G

2747708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27326022-T-A

2748067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27326224-A-G

2748076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27326233-G-C

2748121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27326296-G-A

2748202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27326362-G-T

2748251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27326409-G-A

2748288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27326443-C-G

2748289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27326444-T-A

2748289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27326444-T-G

2748443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27326561-T-C

2748530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27326625-T-C

2748554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27326652-A-G

2748581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27326677-T-C

2769166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27344430-C-T

2769333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27344601-A-G

2769386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27344650-A-T

2771122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27344942-G-A

2771122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27344942-G-C

2771156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27344978-A-G

2771208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27345029-C-T

2771332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27345187-C-T

2771422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27345273-T-C

2771452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27345305-T-C

2771749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27345614-T-C

2771803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27345665-T-C

2771914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27345765-C-T

2772027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27345865-G-C

2772095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27345946-T-C

2772145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27345992-T-A

2779092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27350765-C-G

2779092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27350765-C-T

2779102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27350775-A-G

2779440-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27351090-T-A

2779443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27351093-C-G

2779443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27351093-C-T

2779946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27351236-T-G

http://identifiers.org/hco/9/GRCh38#2779980-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27351279-A-C

2779980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27351279-A-G

2780018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27351315-G-A

2785009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27352700-T-G

http://identifiers.org/hco/9/GRCh38#2785058-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27352747-A-C

2785134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27352825-G-C

2785137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27352828-G-A

2785232-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27352928-T-G

2785248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27352944-A-T

2785573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27353182-A-G

2785785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27353391-C-G

2786060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27353660-T-A

2786062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27353662-G-A

2786102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27353693-G-A

2788190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27354153-G-A

2788190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27354153-G-C

2788202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27354165-T-C

http://identifiers.org/hco/9/GRCh38#2788378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27355071-A-C

2788487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27355171-T-C

2788489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27355173-T-C

2788565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27355241-C-T

2788737-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27355371-A-T

2788970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27355583-A-G

2789112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27355709-C-T

2789196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27355772-G-A

2789196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27355772-G-C

2789197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27355773-C-T

http://identifiers.org/hco/9/GRCh38#2789254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27355830-C-A

2789266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27355843-C-T

2789311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27355886-G-A

2789446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27356012-T-C

2789476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27356042-G-A

2789506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27356066-G-A

2789817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27356699-G-A

2789817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27356699-G-C

2790112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27356957-C-G

2790172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27357013-C-G

2790172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27357013-C-T

2793043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27358616-C-G

2793156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27358726-T-G

2793169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27358742-T-A

2793261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27358823-C-T

2793374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27358938-G-A

2793480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27359041-C-T

2793526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27359086-T-C

2794070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27360337-A-G

2794071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27360338-C-T

2796039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27362684-C-T

2796126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27362766-T-C

2796198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27362826-C-G

2796304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27362931-C-T

2796906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27363558-G-A

2796906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27363558-G-C

2797181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27363779-C-T

2798195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27364002-G-A

2798195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27364002-G-C

2798212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27364027-C-T

2798234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27364049-G-A

2798280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27364098-G-A

2798685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27364510-A-T

2798804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27364615-C-T

2798816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27364625-G-A

2798852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27364667-C-T

2799049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27364841-C-T

2802901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27366321-A-T

2803105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27366511-C-T

2803321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27366679-G-A

2803326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27366684-G-A

2803341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27366702-G-A

2803409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27366762-G-C

2803607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27366940-T-C

2803672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27367009-G-A

2803679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27367016-C-G

2803713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27367047-C-G

http://identifiers.org/hco/9/GRCh38#2803728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27367058-C-A

2803786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27367116-C-T

2803812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27367139-C-G

2803827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27367154-A-T

2803859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27367181-C-T

http://identifiers.org/hco/9/GRCh38#2804028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27367352-C-A

2804041-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27367365-T-A

2804041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27367365-T-C

http://identifiers.org/hco/9/GRCh38#2804043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27367367-C-A

2804043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27367367-C-T

2804071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27367388-T-C

http://identifiers.org/hco/9/GRCh38#2804084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27367401-A-C

2804084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27367401-A-G

http://identifiers.org/hco/9/GRCh38#2804134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27367423-C-A

2804134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27367423-C-T

2804171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27367460-A-G

2804171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27367460-A-T

2804196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27367485-T-C

http://identifiers.org/hco/9/GRCh38#2804215-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27367497-A-C

2804215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27367497-A-G

2804227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27367509-T-C

2804228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27367510-A-G

2804253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27367534-C-T

2804306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 27367560-C-G

http://identifiers.org/hco/9/GRCh38#2804333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, stop_lost
orthologous variants: http://identifiers.org/mco/19/GRCm39#27367583-A-C

2804334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27367584-T-C

2804338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27367588-C-G

2804383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27367633-G-A

2804383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27367633-G-C

2804383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27367633-G-T

2804445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27367695-G-A

2804445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27367695-G-T

2804480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27367738-A-G

http://identifiers.org/hco/9/GRCh38#2804527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27367781-C-A

2804527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27367781-C-G

2804527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27367781-C-T

http://identifiers.org/hco/9/GRCh38#2804581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27367835-C-A

2804581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27367835-C-T

2804601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27367855-A-G

2804601-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27367855-A-T

2804878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27368640-C-T

2804966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27368727-C-T

2804976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27368737-A-G

2805003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27368768-T-C

2805015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27368780-C-G

2805015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27368780-C-T

2805022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27368787-G-C

2805134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27368866-C-T

2805759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27369484-T-C

2805854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27369566-G-A

2805857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27369569-C-G

2805857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27369569-C-T

2805951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27369660-C-T

2806130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27369957-G-A

2806644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27370762-G-A

2806901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27370985-G-A

2807701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27371549-G-A

2807701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27371549-G-T

2807932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27371756-C-T

2808072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27371811-T-A

2808120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27371859-A-T

2808173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27371911-C-G

2808177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27371915-C-G

2808309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27372030-C-T

2808696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27372406-G-C

2808759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27372462-C-T

2808761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27372464-T-C

2808919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27372615-T-C

2810446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, undefined
orthologous variants: 27373797-G-A

2810446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, undefined
orthologous variants: 27373797-G-C

2810446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, undefined
orthologous variants: 27373797-G-T

http://identifiers.org/hco/9/GRCh38#2810583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27373910-A-C

2810583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27373910-A-G

2810816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27374087-A-G

2811210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27374448-G-T

2811268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27374503-T-C

2811268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27374503-T-G

2811279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27374514-C-T

2811285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27376209-G-A

2811285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27376209-G-T

2811299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27376223-T-A

2811299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27376223-T-C

2811343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27376264-G-T

http://identifiers.org/hco/9/GRCh38#2811454-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27376375-A-C

2811460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: synonymous variant
orthologous variants: 27376381-A-G

2811472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: stop gained
orthologous variants: 27376393-A-T

2811495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: missense variant
orthologous variants: 27376416-C-G

2811495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: missense variant
orthologous variants: 27376416-C-T

http://identifiers.org/hco/9/GRCh38#2811601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27376523-C-A

2811601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27376523-C-G

2811601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27376523-C-T

2811623-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27376540-T-A

http://identifiers.org/hco/9/GRCh38#2811626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27376543-C-A

2811626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27376543-C-T

2811639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27376546-G-C

2811639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27376546-G-T

2811704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27376609-T-C

2811715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27376617-T-A

2811987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27376907-G-A

2812071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27376989-G-C

2812071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27376989-G-T

2812107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27377002-A-T

http://identifiers.org/hco/9/GRCh38#2812165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27377055-A-C

2812165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27377055-A-T

2812195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27377060-G-C

2812227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: missense variant
orthologous variants: 27377086-C-G

2812281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: missense variant
orthologous variants: 27377140-G-A

2812281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: missense variant
orthologous variants: 27377140-G-C

2812832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27377504-G-A

2812844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27377516-C-T

2812859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27377531-G-C

2814467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27378982-T-C

2817750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27387388-G-C

2817751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27387389-T-G

2817809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27387450-C-G

2817848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27387488-C-T

2817854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27387494-T-C

http://identifiers.org/hco/9/GRCh38#2817868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27387508-C-A

2818256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27387901-T-C

2818672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27388275-T-C

2818697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27388300-G-A

2818697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27388300-G-C

2818809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27388407-A-G

2819056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27388616-A-G

2819358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27388895-A-G

2819476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27389004-C-T

2819846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27389409-C-T

2819866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27389429-C-T

http://identifiers.org/hco/9/GRCh38#2819965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27389537-C-A

2819965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27389537-C-T

2819967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27389539-A-G

http://identifiers.org/hco/9/GRCh38#2819980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27389551-C-A

2819980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27389551-C-G

2819980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27389551-C-T

2820140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27389802-T-C

2820147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27389809-T-C

http://identifiers.org/hco/9/GRCh38#2820176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27389883-C-A

http://identifiers.org/hco/9/GRCh38#2820194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27390004-C-A

2820194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27390004-C-T

2820213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27390024-A-G

2820234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27390044-G-A

2820234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27390044-G-T

2820277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27390107-T-C

2820462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27390276-C-G

2820602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27390387-T-C

2820631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27390422-T-C

2820631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27390422-T-G

2820653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27390457-T-C

2821559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27391064-C-G

2821602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27391104-G-A

2821678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27391169-A-G

2821695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27391186-T-C

2821750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27391235-G-A

2822053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27391500-C-T

2822177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27391719-G-A

2822233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27391768-G-A

2822527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27392095-G-A

2822527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27392095-G-C

2822622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27392189-T-C

2822650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27392216-A-G

2822678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27392240-C-G

2822864-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27392315-T-A

2822864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27392315-T-C

2822866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27392317-G-A

2822866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27392317-G-C

2823266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27392731-C-T

http://identifiers.org/hco/9/GRCh38#2823407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27392875-C-A

2823407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27392875-C-T

2823444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27392902-C-T

2823552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27393037-G-C

2823564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27393049-T-G

http://identifiers.org/hco/9/GRCh38#2823654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27393162-A-C

2823701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27393199-T-C

2823739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27393234-A-G

2823761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27393266-T-A

2823761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27393266-T-C

2823799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: synonymous variant
orthologous variants: 27393304-A-G

2823799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: stop gained
orthologous variants: 27393304-A-T

2823811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: synonymous variant
orthologous variants: 27393316-T-C

2823853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27393358-T-A

2823853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27393358-T-C

2823863-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27393368-T-A

2823876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27393381-A-G

2823877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27393382-T-C

2823890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27393395-G-A

2823890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27393395-G-T

2823891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27393396-T-A

2823891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27393396-T-C

2823906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27393411-A-G

2824093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27393589-T-C

2824096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27393592-C-T

2824138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27393621-T-A

2824515-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27393959-T-A

2824523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27393967-A-T

2824570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27394002-G-T

2824579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27394011-G-A

2824579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27394011-G-T

http://identifiers.org/hco/9/GRCh38#2824585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27394017-C-A

2824585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27394017-C-G

2824585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27394017-C-T

http://identifiers.org/hco/9/GRCh38#2824616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27394050-A-C

http://identifiers.org/hco/9/GRCh38#2824655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27394099-C-A

2824655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27394099-C-T

2824663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27394112-T-A

2824663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27394112-T-C

2824664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27394113-A-G

2824667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27394116-G-A

2824667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27394116-G-C

2824667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27394116-G-T

2824670-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27394119-T-A

2824670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27394119-T-C

2824729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: synonymous variant
orthologous variants: 27394147-A-G

2824876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27394271-A-G

2824888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27394283-A-G

2824918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27394312-G-A

2824918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27394312-G-T

2824934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27394327-T-C

2824939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27394332-A-G

http://identifiers.org/hco/9/GRCh38#2824947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27394346-C-A

2825004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27394387-C-T

2825063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27394445-C-T

2825287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27394644-T-G

2826010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27394781-C-T

2826318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27395398-T-A

http://identifiers.org/hco/9/GRCh38#2826615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27395685-A-C

2826635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27395710-T-C

2826732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27395807-G-A

2826732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27395807-G-C

2826732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27395807-G-T

2826751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27395822-T-G

2826893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27395962-T-C

http://identifiers.org/hco/9/GRCh38#2826993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27396059-C-A

2826993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27396059-C-T

2826994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27396060-G-A

2826994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27396060-G-T

2826996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27396062-A-G

2826996-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27396062-A-T

2826997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27396063-C-T

http://identifiers.org/hco/9/GRCh38#2827031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27396114-C-A

2827031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27396114-C-T

2827033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27396124-C-T

http://identifiers.org/hco/9/GRCh38#2827061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27396183-C-A

2827061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27396183-C-G

2827080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: missense variant
orthologous variants: 27396202-A-G

2827080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: missense variant
orthologous variants: 27396202-A-T

http://identifiers.org/hco/9/GRCh38#2827127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27396249-C-A

2827127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: synonymous variant
orthologous variants: 27396249-C-T

2827130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: synonymous variant
orthologous variants: 27396252-T-C

2827139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: synonymous variant
orthologous variants: 27396261-A-G

http://identifiers.org/hco/9/GRCh38#2827166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27396288-A-C

http://identifiers.org/hco/9/GRCh38#2827199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27396315-C-A

2827199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27396315-C-G

2827199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27396315-C-T

2827202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27396318-T-A

2827213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27396329-C-G

2827213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27396329-C-T

2827218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27396334-A-G

2827372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27396480-A-T

2827546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27396647-C-T

2827564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27396664-A-G

2827658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27396760-G-A

2827658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27396760-G-C

2827790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27396885-A-G

2827790-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27396885-A-T

http://identifiers.org/hco/9/GRCh38#2828390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27397141-C-A

2828401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27397151-T-C

2828401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27397151-T-G

2828484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27397235-G-C

2828484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27397235-G-T

http://identifiers.org/hco/9/GRCh38#2828542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27397293-C-A

2828558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27397309-T-C

2828560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27397311-G-A

2828560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27397311-G-T

http://identifiers.org/hco/9/GRCh38#2828653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27397396-A-C

2828663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27397406-C-T

2828689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27397432-A-G

http://identifiers.org/hco/9/GRCh38#2828775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27397518-C-A

2828775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27397518-C-G

2828775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27397518-C-T

http://identifiers.org/hco/9/GRCh38#2828803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27397540-C-A

2828803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27397540-C-G

2828803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27397540-C-T

http://identifiers.org/hco/9/GRCh38#2828805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27397542-C-A

2828805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27397542-C-G

2828875-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27397603-A-T

http://identifiers.org/hco/9/GRCh38#2828900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27397646-C-A

2828900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27397646-C-T

2828929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27397713-T-C

2829278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27398216-C-T

2829371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27398302-A-G

2829467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27398390-C-T

2829538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27398452-G-A

2829657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27398582-T-C

http://identifiers.org/hco/9/GRCh38#2829676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27398599-C-A

2829676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27398599-C-G

http://identifiers.org/hco/9/GRCh38#2829684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27398607-A-C

2829684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27398607-A-G

http://identifiers.org/hco/9/GRCh38#2829691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27398614-C-A

2830800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27399609-G-C

2831041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27399835-A-G

2831054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27399848-G-A

2831054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27399848-G-C

2831054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27399848-G-T

2831080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27399881-G-A

2831085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27399886-C-T

2831119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27399941-A-T

2831132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27399954-A-G

2831132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27399954-A-T

2831139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27399961-G-A

2831139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27399961-G-T

http://identifiers.org/hco/9/GRCh38#2831245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27400048-A-C

2833317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27400862-C-T

2833515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27401042-T-C

2833807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27401333-C-T

2833831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27401356-C-T

2833890-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27401412-T-G

http://identifiers.org/hco/9/GRCh38#2833913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27401435-C-A

2833913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27401435-C-T

2833933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27401455-C-T

2833948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27401469-T-C

2834195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27401762-A-G

2834447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27402107-A-G

2834459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27402119-A-T

http://identifiers.org/hco/9/GRCh38#2834495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27402153-C-A

2834497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27402155-T-C

2834595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27402273-G-A

2834698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27402424-T-C

2834700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27402426-T-C

2834776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27402502-T-C

http://identifiers.org/hco/9/GRCh38#2834782-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27402508-A-C

2834826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27402546-G-A

2834905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27402646-A-G

2834932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27402669-T-A

2834932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27402669-T-C

2835004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27402738-G-A

2835090-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27402829-T-G

2837032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27403043-A-G

http://identifiers.org/hco/9/GRCh38#2837056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27403075-C-A

2837056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27403075-C-G

2837056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27403075-C-T

2837152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27403167-G-A

2837152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27403167-G-C

2837162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27403177-G-C

2837162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27403177-G-T

2837352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: synonymous variant
orthologous variants: 27403368-A-G

2837352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: synonymous variant
orthologous variants: 27403368-A-T

2837365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: missense variant
orthologous variants: 27403381-A-G

2837459-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27403476-T-A

2837459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27403476-T-C

2837459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27403476-T-G

2837492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27403509-T-G

http://identifiers.org/hco/9/GRCh38#2837505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27403522-C-A

2837505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27403522-C-T

2837552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27403565-G-A

2837552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27403565-G-C

2837552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27403565-G-T

http://identifiers.org/hco/9/GRCh38#2838309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27404311-C-A

2838309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27404311-C-T

2838376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27404379-C-G

http://identifiers.org/hco/9/GRCh38#2838597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27404605-C-A

2838642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27404648-T-C

2838707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27404710-T-C

http://identifiers.org/hco/9/GRCh38#2838742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27404732-C-A

2838805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27404748-A-G

2838905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27404831-G-C

2839080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27404983-T-C

2839092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27404993-T-A

2839283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27405162-T-C

2839401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27405272-A-G

2839472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27405495-C-T

2839515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27405538-T-C

2839521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27405544-C-G

2839548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27405552-C-T

2839708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27405698-T-C

2840119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27406122-C-T

http://identifiers.org/hco/9/GRCh38#2843919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27407047-C-A

2843919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27407047-C-T

2843930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27407058-A-G

2843956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27407105-A-G

2843956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27407105-A-T

2844011-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27407162-T-A

2844011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron variant
orthologous variants: 27407162-T-C

2844032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, undefined
orthologous variants: 27407179-C-G

2844032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, undefined
orthologous variants: 27407179-C-T

2844033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: intron_variant, undefined
orthologous variants: 27407180-T-C

2844056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 27407203-G-A

2844056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 27407203-G-T

2844057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 27407204-A-T

http://identifiers.org/hco/9/GRCh38#2844074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#27407216-A-C

2844074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 27407216-A-G

2844077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 27407219-G-A

2844077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 27407219-G-T

2844088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 27407230-G-A

2844088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 27407230-G-C

2844088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 27407230-G-T

http://identifiers.org/hco/9/GRCh38#2844090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#27407232-C-A

2844090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29676
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 27407232-C-T