6651955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 72106207-G-A

6651955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 72106207-G-T

http://identifiers.org/hco/17/GRCh38#6651964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72106216-C-A

6651964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 72106216-C-G

6651964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 72106216-C-T

6651990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 72106242-G-A

6651990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 72106242-G-T

6652030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 72106324-G-A

6652030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 72106324-G-T

6652083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 72106377-G-A

http://identifiers.org/hco/17/GRCh38#6652105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72106399-C-A

6652105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 72106399-C-G

6652105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 72106399-C-T

6652147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 72106441-G-A

6652147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 72106441-G-T

http://identifiers.org/hco/17/GRCh38#6652173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72106467-C-A

6652480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 72106717-C-G

6652555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 72106790-G-T

6652645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 72106888-A-G

6652702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 72106950-G-A

6652702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 72106950-G-T

http://identifiers.org/hco/17/GRCh38#6652900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72107155-A-C

6652900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 72107155-A-T

http://identifiers.org/hco/17/GRCh38#6652961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72107207-C-A

6661493-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72111616-T-A

6661493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72111616-T-C

6661493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72111616-T-G

http://identifiers.org/hco/17/GRCh38#6661563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72111652-C-A

6661563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72111652-C-T

6661609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72111694-T-G

6661733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72111808-A-T

6661807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72111879-G-T

6661848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72111915-A-T

6661868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72111935-G-T

http://identifiers.org/hco/17/GRCh38#6662369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72112230-C-A

http://identifiers.org/hco/17/GRCh38#6662371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72112232-C-A

6662375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72112236-G-A

6662521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72112419-A-T

http://identifiers.org/hco/17/GRCh38#6662639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72112531-C-A

6662692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72112581-T-C

6662745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72112625-G-A

6662780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72112661-G-T

6662959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72113283-T-C

http://identifiers.org/hco/17/GRCh38#6663192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72113444-A-C

6663594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72113830-G-C

6663645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72113879-G-A

6664167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: -G-A

6666103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72115786-T-C

6666119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72115802-C-G

http://identifiers.org/hco/17/GRCh38#6666130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72115813-C-A

6666138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72115820-A-T

6666205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72115883-C-T

http://identifiers.org/hco/17/GRCh38#6666249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72115926-C-A

6666904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72116343-T-C

http://identifiers.org/hco/17/GRCh38#6667192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72116570-C-A

6667255-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72116640-A-T

6669102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72117084-C-T

6669124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72117106-T-C

6669507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72117468-G-A

6669673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72117608-T-C

6669768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72117710-C-T

6669787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72117729-C-T

6670073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72118012-C-T

http://identifiers.org/hco/17/GRCh38#6670315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72118230-C-A

6670315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72118230-C-T

6670657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72118383-G-A

6670844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72118576-G-A

6671015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72118732-C-T

6671035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72118751-C-T

6671262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72118906-G-A

6671416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72119031-G-A

6671639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72119255-C-T

6671747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72119349-C-T

6671782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72119384-C-T

6671895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72119479-C-T

6672374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72119744-G-A

6672400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72119763-A-G

http://identifiers.org/hco/17/GRCh38#6672690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72120042-C-A

6674015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72120349-T-C

6674040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72120374-G-C

6674323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72120623-G-A

6674425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72120726-C-T

6674754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72121062-G-T

6674765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72121072-A-G

6674767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72121074-C-T

http://identifiers.org/hco/17/GRCh38#6675364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72121675-A-C

6675376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72121684-C-G

6675376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72121684-C-T

6675377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72121685-G-A

6675377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72121685-G-C

http://identifiers.org/hco/17/GRCh38#6675478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72121788-A-C

6675894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72122128-C-T

6675907-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72122141-T-G

6676301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72123759-C-T

6676359-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72123830-T-A

6676359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72123830-T-C

6676585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72124041-G-A

6676671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72124153-G-T

http://identifiers.org/hco/17/GRCh38#6676715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72124198-C-A

6676715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72124198-C-G

6677113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72124586-A-G

6677306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72124757-C-T

6677428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72124865-T-C

6677572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72124968-T-C

6678075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72125350-T-C

6678110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72125385-G-A

6678110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72125385-G-T

6678409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72125635-C-T

6678442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72125678-A-G

6678587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72125839-G-C

6678587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72125839-G-T

6678609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72125980-A-G

6678634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72126067-G-A

http://identifiers.org/hco/17/GRCh38#6679273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72126693-C-A

http://identifiers.org/hco/17/GRCh38#6679276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72126696-A-C

6679345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72126749-T-C

6680134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72129034-G-A

6680317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72129214-G-A

6680607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72129529-G-A

6680663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72129556-C-T

6680691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72129584-G-A

6680691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72129584-G-C

6680691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72129584-G-T

6680861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72129718-G-A

6681000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72130018-G-A

6681000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72130018-G-C

6681061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72130096-T-G

6681317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72130304-C-G

6682069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72130734-G-A

6682200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72130841-G-A

6682437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72131051-C-T

6682453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72131075-T-C

6682638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72131260-G-A

6682811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72131435-C-T

6682880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72131499-C-T

6682891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72131510-C-T

6683390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72131949-C-T

6683656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72132475-T-C

6684102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72132348-G-A

6684102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72132348-G-T

6684176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72132395-C-T

6684410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72132618-A-G

6684533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72132726-A-T

6684549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72132741-A-G

http://identifiers.org/hco/17/GRCh38#6684579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72132771-A-C

http://identifiers.org/hco/17/GRCh38#6684683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72132873-C-A

6684683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72132873-C-T

http://identifiers.org/hco/17/GRCh38#6684793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72132980-C-A

6684793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72132980-C-G

http://identifiers.org/hco/17/GRCh38#6684839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72133026-C-A

6684839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72133026-C-G

6684875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72133069-A-G

6684941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72133134-A-G

6684974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72133165-A-G

6685096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72133230-C-T

6685104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72133238-A-G

6685332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72133477-T-C

6685333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72133478-A-G

http://identifiers.org/hco/17/GRCh38#6685396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72133542-C-A

6685396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72133542-C-T

http://identifiers.org/hco/17/GRCh38#6685422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72133566-C-A

6685422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72133566-C-T

http://identifiers.org/hco/17/GRCh38#6685437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72133570-C-A

6685482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72133616-T-A

6685485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72133619-G-A

6685485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72133619-G-T

6685537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72133692-G-A

6685537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72133692-G-T

6685589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72133736-T-C

http://identifiers.org/hco/17/GRCh38#6685596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72133743-C-A

6685643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72133787-G-A

http://identifiers.org/hco/17/GRCh38#6685667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72133811-C-A

6685673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72133817-G-T

6685736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72133879-A-G

http://identifiers.org/hco/17/GRCh38#6685754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72133897-C-A

6685754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72133897-C-T

6685782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72133915-T-C

6685782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72133915-T-G

6685813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72133931-G-A

6685813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72133931-G-T

6685814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72133932-G-A

6685814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72133932-G-C

6685814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72133932-G-T

6685860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72133990-A-G

6685885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134017-G-A

6685885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134017-G-T

6685931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134066-G-A

6685931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134066-G-T

http://identifiers.org/hco/17/GRCh38#6685937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72134072-C-A

6685937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134072-C-T

6685977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134110-G-A

6685977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134110-G-T

http://identifiers.org/hco/17/GRCh38#6686018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72134152-C-A

6686018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134152-C-T

http://identifiers.org/hco/17/GRCh38#6686019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72134153-C-A

6686019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134153-C-T

6686051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134185-T-C

6686051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134185-T-G

http://identifiers.org/hco/17/GRCh38#6686107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72134224-C-A

6686107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134224-C-G

6686108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134225-A-G

6686108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134225-A-T

6686118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134235-G-A

6686142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134259-G-T

6686263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 72134387-T-C

6686513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134573-G-A

6686513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134573-G-T

6686550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134609-G-T

http://identifiers.org/hco/17/GRCh38#6686685-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72134681-A-C

6686685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134681-A-G

6686685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134681-A-T

http://identifiers.org/hco/17/GRCh38#6686746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72134709-C-A

6686746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134709-C-T

6686766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134729-G-A

6686766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134729-G-T

http://identifiers.org/hco/17/GRCh38#6686788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72134751-C-A

6686788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134751-C-T

6686894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134858-G-T

6686982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134949-G-A

6686982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134949-G-C

6686982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72134949-G-T

http://identifiers.org/hco/17/GRCh38#6687045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72135020-C-A

6687045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72135020-C-T

6687068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72135043-T-C

http://identifiers.org/hco/17/GRCh38#6687113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72135069-C-A

6687113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72135069-C-T

http://identifiers.org/hco/17/GRCh38#6687186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72135120-C-A

6687186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72135120-C-T

http://identifiers.org/hco/17/GRCh38#6687429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72135358-C-A

6687460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72135885-A-G

6687460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72135885-A-T

6687506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 72135932-G-A

6687872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72136286-G-A

6687872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72136286-G-C

6687872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72136286-G-T

http://identifiers.org/hco/17/GRCh38#6687897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72136313-C-A

http://identifiers.org/hco/17/GRCh38#6687898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72136314-A-C

6687898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72136314-A-G

6687900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72136316-G-T

http://identifiers.org/hco/17/GRCh38#6687955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72136357-C-A

http://identifiers.org/hco/17/GRCh38#6687979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72136380-C-A

http://identifiers.org/hco/17/GRCh38#6688088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72136458-C-A

6688088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72136458-C-T

6688240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72136584-C-T

6688259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72136595-G-T

http://identifiers.org/hco/17/GRCh38#6689492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72137022-C-A

6689492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72137022-C-T

6689597-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72137124-A-T

6689757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72137421-A-T

6690127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72137723-T-A

6690164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72137761-T-C

6690595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72138306-C-G

6690595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72138306-C-T

6690631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72138346-G-A

6690631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72138346-G-T

6690633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72138348-T-C

6690938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 72138652-G-T

6691008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72138718-G-A

6691008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72138718-G-C

6691008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72138718-G-T

http://identifiers.org/hco/17/GRCh38#6691044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72138752-A-C

6691257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72139383-T-C

6691796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72139882-C-T

http://identifiers.org/hco/17/GRCh38#6692494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72141133-C-A

6692758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72141342-T-C

6692783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72141362-T-C

6692783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72141362-T-G

6692801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72141380-G-A

6692801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72141380-G-T

6693080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 72141588-T-G

6693149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 72141657-T-C

http://identifiers.org/hco/17/GRCh38#6693184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72141692-C-A

6693199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72141707-A-G